RDF of MGI data
abnormal cochlear nerve compound action potential
http://purl.obolibrary.org/obo/MP_0004415
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abnormal cochlear nerve compound action potential
rdfs:label
http://www.w3.org/2000/01/rdf-schema#label
abnormal cochlear nerve compound action potential
表現型アノテーション
http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype
abnormal cochlear nerve compound action potential_Cdh23<v>/Cdh23<+>,Myo7a<4626SB>/Myo7a<+>
http://metadb.riken.jp/0004415IBALBcRl47BSRlCBACaCdh23vCdh23Myo7a4626SBMyo7aMyo7aCdh23vCdh23Myo7a4626SB
abnormal cochlear nerve compound action potential_Chrna9<tm1Bedv>/Chrna9<tm1Bedv>
http://metadb.riken.jp/0004415ECB129S1Chrna9tm1BedvorI129S1SvorI129S1SvCBACaJChrna9tm1BedvChrna9tm1BedvChrna9tm1Bedv
abnormal cochlear nerve compound action potential_Cdh23<v>/Cdh23<+>
http://metadb.riken.jp/0004415IBALBcRl47BSRlCBACaCdh23vCdh23Cdh23vCdh23
abnormal cochlear nerve compound action potential_Fgfr1<Hspy>/Fgfr1<+>
http://metadb.riken.jp/0004415C3HeBFeJHspyFgfr1HspyFgfr1Fgfr1HspyFgfr1
abnormal cochlear nerve compound action potential_Atp2b2<dfw>/Atp2b2<+>
http://metadb.riken.jp/0004415C3HHeJAtp2b2dfwJAtp2b2dfwAtp2b2Atp2b2Atp2b2dfw
abnormal cochlear nerve compound action potential_Otoa<tm1Gpr>/Otoa<tm1Gpr>
http://metadb.riken.jp/0004415I129SSvEvOtoatm1GprOtoatm1GprOtoatm1Gpr
abnormal cochlear nerve compound action potential_Myo7a<4626SB>/Myo7a<+>
http://metadb.riken.jp/0004415IBALBcRl47BSRlCBACaMyo7a4626SBMyo7aMyo7aMyo7a4626SB
abnormal cochlear nerve compound action potential_Thrb<tm1Df>/Thrb<tm1Df>
http://metadb.riken.jp/0004415I129S1SvC57BL6JFVBNJThrbtm1DfThrbtm1DfThrbtm1Df
abnormal cochlear nerve compound action potential_Pcdh15<tm1.1Ugds>/Pcdh15<tm1.1Ugds>,Myo15<tm1.1(cre)Ugds>/Myo15<+>
http://metadb.riken.jp/0004415I129S1SvImJC57BL6JPcdh15tm11UgdsPcdh15tm11UgdsMyo15tm11creUgdsMyo15Pcdh15tm11UgdsMyo15Myo15tm11creUgds
表現型アノテーション
http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype
abnormal cochlear nerve compound action potential in RBRC00333
http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1017080
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