@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP436799.RAPtK6LvEFJexHFq16bHBnUuyoTDG9arP07Zb69bSJRDQ130_head { this: np:hasAssertion dgn-np:NP436799.RAPtK6LvEFJexHFq16bHBnUuyoTDG9arP07Zb69bSJRDQ130_assertion; np:hasProvenance dgn-np:NP436799.RAPtK6LvEFJexHFq16bHBnUuyoTDG9arP07Zb69bSJRDQ130_provenance; np:hasPublicationInfo dgn-np:NP436799.RAPtK6LvEFJexHFq16bHBnUuyoTDG9arP07Zb69bSJRDQ130_publicationInfo; a np:Nanopublication . dgn-np:NP436799.RAPtK6LvEFJexHFq16bHBnUuyoTDG9arP07Zb69bSJRDQ130_assertion a np:Assertion . dgn-np:NP436799.RAPtK6LvEFJexHFq16bHBnUuyoTDG9arP07Zb69bSJRDQ130_provenance a np:Provenance . dgn-np:NP436799.RAPtK6LvEFJexHFq16bHBnUuyoTDG9arP07Zb69bSJRDQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP436799.RAPtK6LvEFJexHFq16bHBnUuyoTDG9arP07Zb69bSJRDQ130_assertion { miriam-gene:27123 a ncit:C16612 . lld:C0007134 a ncit:C7057 . dgn-gda:DGN11e14a9a7e11916e0a78d4c50533f775 sio:SIO_000628 miriam-gene:27123, lld:C0007134; a sio:SIO_001121 . } dgn-np:NP436799.RAPtK6LvEFJexHFq16bHBnUuyoTDG9arP07Zb69bSJRDQ130_provenance { dgn-np:NP436799.RAPtK6LvEFJexHFq16bHBnUuyoTDG9arP07Zb69bSJRDQ130_assertion dcterms:description "[including Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:19562778; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP436799.RAPtK6LvEFJexHFq16bHBnUuyoTDG9arP07Zb69bSJRDQ130_publicationInfo { this: dcterms:created "2014-10-02T12:36:18+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }