Javascript doit fonctionner ! Activez-le et rechargez cette page.
Le Rézo de JeuxDeMots
• Types de relations
• Types de noeuds
• Consolider
le terme
  Options  
             

  Filtrage type relations : +   - (ex: 4, 12, 18, 36, 444, 555, 777)
  Filtrage valeur :          min   max
  Filtrage type noeuds :   +   - (ex: 4, 6, 8, 9, 10, 12, 18, 36, 444, 555, 777)

  Présentation de sortie :   (ex: -rien-, cloud, nicecloud)
 

'en:structural variant reported start-end:numrange:pt:^patient:qn'
(id=12532143 ; fe=en:structural variant reported start-end:numrange:pt:^patient:qn ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=316 creation date=2019-04-29 touchdate=2024-09-18 00:02:50.000)
≈ 10 relations sortantes

  1. en:structural variant reported start-end:numrange:pt:^patient:qn -- r_associated #0: 25 / 1 -> en:structural
    n1=en:structural variant reported start-end:numrange:pt:^patient:qn | n2=en:structural | rel=r_associated | relid=0 | w=25
  2. en:structural variant reported start-end:numrange:pt:^patient:qn -- r_associated #0: 20 / 0.8 -> en:allelic frequency:number fraction:point in time:^patient:quantitative
    n1=en:structural variant reported start-end:numrange:pt:^patient:qn | n2=en:allelic frequency:number fraction:point in time:^patient:quantitative | rel=r_associated | relid=0 | w=20
  3. en:structural variant reported start-end:numrange:pt:^patient:qn -- r_associated #0: 20 / 0.8 -> en:bcr-abl1 b3a2 fusion protein:prthr:pt:bld/tiss:ord:molgen
    n1=en:structural variant reported start-end:numrange:pt:^patient:qn | n2=en:bcr-abl1 b3a2 fusion protein:prthr:pt:bld/tiss:ord:molgen | rel=r_associated | relid=0 | w=20
  4. en:structural variant reported start-end:numrange:pt:^patient:qn -- r_associated #0: 20 / 0.8 -> en:chromosome analysis.interphase:imp:pt:amnio fld:nar:fish
    n1=en:structural variant reported start-end:numrange:pt:^patient:qn | n2=en:chromosome analysis.interphase:imp:pt:amnio fld:nar:fish | rel=r_associated | relid=0 | w=20
  5. en:structural variant reported start-end:numrange:pt:^patient:qn -- r_associated #0: 20 / 0.8 -> en:colonies counted:num:pt:amnio fld:qn:molgen
    n1=en:structural variant reported start-end:numrange:pt:^patient:qn | n2=en:colonies counted:num:pt:amnio fld:qn:molgen | rel=r_associated | relid=0 | w=20
  6. en:structural variant reported start-end:numrange:pt:^patient:qn -- r_associated #0: 20 / 0.8 -> en:complex variant:id:pt:^patient:nom
    n1=en:structural variant reported start-end:numrange:pt:^patient:qn | n2=en:complex variant:id:pt:^patient:nom | rel=r_associated | relid=0 | w=20
  7. en:structural variant reported start-end:numrange:pt:^patient:qn -- r_associated #0: 20 / 0.8 -> en:genomic allele start-end:id:pt:^patient:nom
    n1=en:structural variant reported start-end:numrange:pt:^patient:qn | n2=en:genomic allele start-end:id:pt:^patient:nom | rel=r_associated | relid=0 | w=20
  8. en:structural variant reported start-end:numrange:pt:^patient:qn -- r_associated #0: 20 / 0.8 -> en:kir gene allele 2dl3:prthr:pt:bld/tiss:ord:molgen
    n1=en:structural variant reported start-end:numrange:pt:^patient:qn | n2=en:kir gene allele 2dl3:prthr:pt:bld/tiss:ord:molgen | rel=r_associated | relid=0 | w=20
  9. en:structural variant reported start-end:numrange:pt:^patient:qn -- r_associated #0: 20 / 0.8 -> en:kir gene allele 3dl1:prthr:pt:bld/tiss:ord:molgen
    n1=en:structural variant reported start-end:numrange:pt:^patient:qn | n2=en:kir gene allele 3dl1:prthr:pt:bld/tiss:ord:molgen | rel=r_associated | relid=0 | w=20
  10. en:structural variant reported start-end:numrange:pt:^patient:qn -- r_associated #0: 20 / 0.8 -> en:structural variant:type:pt:^patient:nom
    n1=en:structural variant reported start-end:numrange:pt:^patient:qn | n2=en:structural variant:type:pt:^patient:nom | rel=r_associated | relid=0 | w=20
≈ 9 relations entrantes

  1. en:kir gene allele 3dl1:prthr:pt:bld/tiss:ord:molgen --- r_associated #0: 41 --> en:structural variant reported start-end:numrange:pt:^patient:qn
    n1=en:kir gene allele 3dl1:prthr:pt:bld/tiss:ord:molgen | n2=en:structural variant reported start-end:numrange:pt:^patient:qn | rel=r_associated | relid=0 | w=41
  2. en:chromosome analysis.interphase:imp:pt:amnio fld:nar:fish --- r_associated #0: 40 --> en:structural variant reported start-end:numrange:pt:^patient:qn
    n1=en:chromosome analysis.interphase:imp:pt:amnio fld:nar:fish | n2=en:structural variant reported start-end:numrange:pt:^patient:qn | rel=r_associated | relid=0 | w=40
  3. en:kir gene allele 2dl3:prthr:pt:bld/tiss:ord:molgen --- r_associated #0: 38 --> en:structural variant reported start-end:numrange:pt:^patient:qn
    n1=en:kir gene allele 2dl3:prthr:pt:bld/tiss:ord:molgen | n2=en:structural variant reported start-end:numrange:pt:^patient:qn | rel=r_associated | relid=0 | w=38
  4. en:complex variant:id:pt:^patient:nom --- r_associated #0: 32 --> en:structural variant reported start-end:numrange:pt:^patient:qn
    n1=en:complex variant:id:pt:^patient:nom | n2=en:structural variant reported start-end:numrange:pt:^patient:qn | rel=r_associated | relid=0 | w=32
  5. en:genomic allele start-end:id:pt:^patient:nom --- r_associated #0: 31 --> en:structural variant reported start-end:numrange:pt:^patient:qn
    n1=en:genomic allele start-end:id:pt:^patient:nom | n2=en:structural variant reported start-end:numrange:pt:^patient:qn | rel=r_associated | relid=0 | w=31
  6. en:colonies counted:num:pt:amnio fld:qn:molgen --- r_associated #0: 28 --> en:structural variant reported start-end:numrange:pt:^patient:qn
    n1=en:colonies counted:num:pt:amnio fld:qn:molgen | n2=en:structural variant reported start-end:numrange:pt:^patient:qn | rel=r_associated | relid=0 | w=28
  7. en:structural variant:type:pt:^patient:nom --- r_associated #0: 28 --> en:structural variant reported start-end:numrange:pt:^patient:qn
    n1=en:structural variant:type:pt:^patient:nom | n2=en:structural variant reported start-end:numrange:pt:^patient:qn | rel=r_associated | relid=0 | w=28
  8. en:bcr-abl1 b3a2 fusion protein:prthr:pt:bld/tiss:ord:molgen --- r_associated #0: 27 --> en:structural variant reported start-end:numrange:pt:^patient:qn
    n1=en:bcr-abl1 b3a2 fusion protein:prthr:pt:bld/tiss:ord:molgen | n2=en:structural variant reported start-end:numrange:pt:^patient:qn | rel=r_associated | relid=0 | w=27
  9. en:allelic frequency:number fraction:point in time:^patient:quantitative --- r_associated #0: 26 --> en:structural variant reported start-end:numrange:pt:^patient:qn
    n1=en:allelic frequency:number fraction:point in time:^patient:quantitative | n2=en:structural variant reported start-end:numrange:pt:^patient:qn | rel=r_associated | relid=0 | w=26
Le service Rézo permet d'énumérer les relations existant pour un terme. Ce service est interrogeable par programme.
Projet JeuxDeMots - url: http://www.jeuxdemots.org
contact: mathieu.lafourcade@lirmm.fr