≈ 38 relations sortantes
- IAC --
r_associated #0: 40 / 1 ->
fécondation
n1=IAC | n2=fécondation | rel=r_associated | relid=0 | w=40
- IAC --
r_associated #0: 37 / 0.925 ->
en:intraconjugual artificial insemination
n1=IAC | n2=en:intraconjugual artificial insemination | rel=r_associated | relid=0 | w=37
- IAC --
r_associated #0: 35 / 0.875 ->
en:intrauterine insemination
n1=IAC | n2=en:intrauterine insemination | rel=r_associated | relid=0 | w=35
- IAC --
r_associated #0: 31 / 0.775 ->
en:AIH
n1=IAC | n2=en:AIH | rel=r_associated | relid=0 | w=31
- IAC --
r_associated #0: 31 / 0.775 ->
en:artificial insemination by partner
n1=IAC | n2=en:artificial insemination by partner | rel=r_associated | relid=0 | w=31
- IAC --
r_associated #0: 30 / 0.75 ->
en:Institut d'Art Contemporain
n1=IAC | n2=en:Institut d'Art Contemporain | rel=r_associated | relid=0 | w=30
- IAC --
r_associated #0: 30 / 0.75 ->
en:Institute of Contemporary Art
n1=IAC | n2=en:Institute of Contemporary Art | rel=r_associated | relid=0 | w=30
- IAC --
r_associated #0: 29 / 0.725 ->
artificielle
n1=IAC | n2=artificielle | rel=r_associated | relid=0 | w=29
- IAC --
r_associated #0: 29 / 0.725 ->
en:IAC
n1=IAC | n2=en:IAC | rel=r_associated | relid=0 | w=29
- IAC --
r_associated #0: 28 / 0.7 ->
en:IUI
n1=IAC | n2=en:IUI | rel=r_associated | relid=0 | w=28
- IAC --
r_associated #0: 27 / 0.675 ->
insémination
n1=IAC | n2=insémination | rel=r_associated | relid=0 | w=27
- IAC --
r_associated #0: 27 / 0.675 ->
insémination artificielle
n1=IAC | n2=insémination artificielle | rel=r_associated | relid=0 | w=27
- IAC --
r_associated #0: 22 / 0.55 ->
intra-conjugale
n1=IAC | n2=intra-conjugale | rel=r_associated | relid=0 | w=22
- IAC --
r_associated #0: 20 / 0.5 ->
en:fecundation
n1=IAC | n2=en:fecundation | rel=r_associated | relid=0 | w=20
- IAC --
r_associated #0: 20 / 0.5 ->
en:pollination
n1=IAC | n2=en:pollination | rel=r_associated | relid=0 | w=20
- IAC --
r_associated #0: 20 / 0.5 ->
IAC 161
n1=IAC | n2=IAC 161 | rel=r_associated | relid=0 | w=20
- IAC --
r_associated #0: 20 / 0.5 ->
IAC 161 Valencia Late
n1=IAC | n2=IAC 161 Valencia Late | rel=r_associated | relid=0 | w=20
- IAC --
r_associated #0: 20 / 0.5 ->
IAC 161 València Late
n1=IAC | n2=IAC 161 València Late | rel=r_associated | relid=0 | w=20
- IAC --
r_associated #0: 20 / 0.5 ->
IAC 161 Valência Late
n1=IAC | n2=IAC 161 Valência Late | rel=r_associated | relid=0 | w=20
- IAC --
r_associated #0: 20 / 0.5 ->
IAC 476
n1=IAC | n2=IAC 476 | rel=r_associated | relid=0 | w=20
- IAC --
r_associated #0: 20 / 0.5 ->
IAC 476 Valencia Taquari
n1=IAC | n2=IAC 476 Valencia Taquari | rel=r_associated | relid=0 | w=20
- IAC --
r_associated #0: 20 / 0.5 ->
IAC 476 València Taquari
n1=IAC | n2=IAC 476 València Taquari | rel=r_associated | relid=0 | w=20
- IAC --
r_associated #0: 20 / 0.5 ->
IAC 476 Valência Taquari
n1=IAC | n2=IAC 476 Valência Taquari | rel=r_associated | relid=0 | w=20
- IAC --
r_associated #0: 20 / 0.5 ->
IAC 489
n1=IAC | n2=IAC 489 | rel=r_associated | relid=0 | w=20
- IAC --
r_associated #0: 20 / 0.5 ->
IAC 489 Valencia FM
n1=IAC | n2=IAC 489 Valencia FM | rel=r_associated | relid=0 | w=20
- IAC --
r_associated #0: 20 / 0.5 ->
IAC 489 Valência FM
n1=IAC | n2=IAC 489 Valência FM | rel=r_associated | relid=0 | w=20
- IAC --
r_associated #0: 15 / 0.375 ->
en:I/E ratio
n1=IAC | n2=en:I/E ratio | rel=r_associated | relid=0 | w=15
- IAC --
r_associated #0: 15 / 0.375 ->
I/E (rapport)
n1=IAC | n2=I/E (rapport) | rel=r_associated | relid=0 | w=15
- IAC --
r_associated #0: 15 / 0.375 ->
IA
n1=IAC | n2=IA | rel=r_associated | relid=0 | w=15
- IAC --
r_associated #0: 15 / 0.375 ->
IAD
n1=IAC | n2=IAD | rel=r_associated | relid=0 | w=15
- IAC --
r_associated #0: 15 / 0.375 ->
IAMP
n1=IAC | n2=IAMP | rel=r_associated | relid=0 | w=15
- IAC --
r_associated #0: 15 / 0.375 ->
ianthinopsie
n1=IAC | n2=ianthinopsie | rel=r_associated | relid=0 | w=15
- IAC --
r_associated #0: 15 / 0.375 ->
IAP
n1=IAC | n2=IAP | rel=r_associated | relid=0 | w=15
- IAC --
r_associated #0: 15 / 0.375 ->
iatrogène
n1=IAC | n2=iatrogène | rel=r_associated | relid=0 | w=15
- IAC --
r_associated #0: 15 / 0.375 ->
insectes (allergie aux)
n1=IAC | n2=insectes (allergie aux) | rel=r_associated | relid=0 | w=15
- IAC --
r_associated #0: 15 / 0.375 ->
rapport
n1=IAC | n2=rapport | rel=r_associated | relid=0 | w=15
- IAC --
r_associated #0: 15 / 0.375 ->
rapport I/E
n1=IAC | n2=rapport I/E | rel=r_associated | relid=0 | w=15
- IAC --
r_associated #0: 10 / 0.25 ->
en:artificial
n1=IAC | n2=en:artificial | rel=r_associated | relid=0 | w=10
| ≈ 45 relations entrantes
- fécondation ---
r_associated #0: 40 -->
IAC
n1=fécondation | n2=IAC | rel=r_associated | relid=0 | w=40
- en:Institut d'Art Contemporain ---
r_associated #0: 39 -->
IAC
n1=en:Institut d'Art Contemporain | n2=IAC | rel=r_associated | relid=0 | w=39
- en:IUI ---
r_associated #0: 36 -->
IAC
n1=en:IUI | n2=IAC | rel=r_associated | relid=0 | w=36
- en:IAC ---
r_associated #0: 35 -->
IAC
n1=en:IAC | n2=IAC | rel=r_associated | relid=0 | w=35
- en:AIH ---
r_associated #0: 34 -->
IAC
n1=en:AIH | n2=IAC | rel=r_associated | relid=0 | w=34
- en:pollination ---
r_associated #0: 30 -->
IAC
n1=en:pollination | n2=IAC | rel=r_associated | relid=0 | w=30
- en:artificial insemination by partner ---
r_associated #0: 29 -->
IAC
n1=en:artificial insemination by partner | n2=IAC | rel=r_associated | relid=0 | w=29
- en:fecundation ---
r_associated #0: 29 -->
IAC
n1=en:fecundation | n2=IAC | rel=r_associated | relid=0 | w=29
- en:Institute of Contemporary Art ---
r_associated #0: 28 -->
IAC
n1=en:Institute of Contemporary Art | n2=IAC | rel=r_associated | relid=0 | w=28
- IAC 161 ---
r_associated #0: 26 -->
IAC
n1=IAC 161 | n2=IAC | rel=r_associated | relid=0 | w=26
- IAC 161 Valencia Late ---
r_associated #0: 26 -->
IAC
n1=IAC 161 Valencia Late | n2=IAC | rel=r_associated | relid=0 | w=26
- IAC 161 València Late ---
r_associated #0: 26 -->
IAC
n1=IAC 161 València Late | n2=IAC | rel=r_associated | relid=0 | w=26
- IAC 161 Valência Late ---
r_associated #0: 26 -->
IAC
n1=IAC 161 Valência Late | n2=IAC | rel=r_associated | relid=0 | w=26
- IAC 476 ---
r_associated #0: 26 -->
IAC
n1=IAC 476 | n2=IAC | rel=r_associated | relid=0 | w=26
- IAC 476 Valencia Taquari ---
r_associated #0: 26 -->
IAC
n1=IAC 476 Valencia Taquari | n2=IAC | rel=r_associated | relid=0 | w=26
- IAC 476 València Taquari ---
r_associated #0: 26 -->
IAC
n1=IAC 476 València Taquari | n2=IAC | rel=r_associated | relid=0 | w=26
- IAC 476 Valência Taquari ---
r_associated #0: 26 -->
IAC
n1=IAC 476 Valência Taquari | n2=IAC | rel=r_associated | relid=0 | w=26
- IAC 489 ---
r_associated #0: 26 -->
IAC
n1=IAC 489 | n2=IAC | rel=r_associated | relid=0 | w=26
- IAC 489 Valencia FM ---
r_associated #0: 26 -->
IAC
n1=IAC 489 Valencia FM | n2=IAC | rel=r_associated | relid=0 | w=26
- IAC 489 Valência FM ---
r_associated #0: 26 -->
IAC
n1=IAC 489 Valência FM | n2=IAC | rel=r_associated | relid=0 | w=26
- en:intrauterine insemination ---
r_associated #0: 26 -->
IAC
n1=en:intrauterine insemination | n2=IAC | rel=r_associated | relid=0 | w=26
- IAC 489 València FM ---
r_associated #0: 25 -->
IAC
n1=IAC 489 València FM | n2=IAC | rel=r_associated | relid=0 | w=25
- Orange Valencia ---
r_associated #0: 25 -->
IAC
n1=Orange Valencia | n2=IAC | rel=r_associated | relid=0 | w=25
- artificielle ---
r_associated #0: 20 -->
IAC
n1=artificielle | n2=IAC | rel=r_associated | relid=0 | w=20
- en:intraconjugual artificial insemination ---
r_associated #0: 20 -->
IAC
n1=en:intraconjugual artificial insemination | n2=IAC | rel=r_associated | relid=0 | w=20
- insémination ---
r_associated #0: 20 -->
IAC
n1=insémination | n2=IAC | rel=r_associated | relid=0 | w=20
- insémination artificielle ---
r_associated #0: 20 -->
IAC
n1=insémination artificielle | n2=IAC | rel=r_associated | relid=0 | w=20
- Fechtner (syndrome de) ---
r_associated #0: 15 -->
IAC
n1=Fechtner (syndrome de) | n2=IAC | rel=r_associated | relid=0 | w=15
- Fécondation ---
r_associated #0: 15 -->
IAC
n1=Fécondation | n2=IAC | rel=r_associated | relid=0 | w=15
- I/E (rapport) ---
r_associated #0: 15 -->
IAC
n1=I/E (rapport) | n2=IAC | rel=r_associated | relid=0 | w=15
- IAMP ---
r_associated #0: 15 -->
IAC
n1=IAMP | n2=IAC | rel=r_associated | relid=0 | w=15
- ianthinopsie ---
r_associated #0: 15 -->
IAC
n1=ianthinopsie | n2=IAC | rel=r_associated | relid=0 | w=15
- iatrogène ---
r_associated #0: 15 -->
IAC
n1=iatrogène | n2=IAC | rel=r_associated | relid=0 | w=15
- en:I/E ratio ---
r_associated #0: 10 -->
IAC
n1=en:I/E ratio | n2=IAC | rel=r_associated | relid=0 | w=10
- en:ianthinopsia ---
r_associated #0: 10 -->
IAC
n1=en:ianthinopsia | n2=IAC | rel=r_associated | relid=0 | w=10
- en:iatrogenic ---
r_associated #0: 10 -->
IAC
n1=en:iatrogenic | n2=IAC | rel=r_associated | relid=0 | w=10
- pollination ---
r_associated #0: 10 -->
IAC
n1=pollination | n2=IAC | rel=r_associated | relid=0 | w=10
- ARTIFICIELLE ---
r_associated #0: 5 -->
IAC
n1=ARTIFICIELLE | n2=IAC | rel=r_associated | relid=0 | w=5
- IA
(insémination artificielle) ---
r_associated #0: 5 -->
IAC
n1=IA (insémination artificielle) | n2=IAC | rel=r_associated | relid=0 | w=5
- Iatrogène ---
r_associated #0: 5 -->
IAC
n1=Iatrogène | n2=IAC | rel=r_associated | relid=0 | w=5
- Insémination artificielle ---
r_associated #0: 5 -->
IAC
n1=Insémination artificielle | n2=IAC | rel=r_associated | relid=0 | w=5
- fécondabilité ---
r_associated #0: 5 -->
IAC
n1=fécondabilité | n2=IAC | rel=r_associated | relid=0 | w=5
- fécondance ---
r_associated #0: 5 -->
IAC
n1=fécondance | n2=IAC | rel=r_associated | relid=0 | w=5
- pollinisation ---
r_associated #0: 5 -->
IAC
n1=pollinisation | n2=IAC | rel=r_associated | relid=0 | w=5
- syndrome de Fechtner ---
r_associated #0: 5 -->
IAC
n1=syndrome de Fechtner | n2=IAC | rel=r_associated | relid=0 | w=5
|