@prefix orcid: . @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:NP56255.RAAEEDEH-AVC3Uq8Rb5d-eRE1sWWxzR11eb1IPTYmFVYg130_head { this: np:hasAssertion dgn-np:NP56255.RAAEEDEH-AVC3Uq8Rb5d-eRE1sWWxzR11eb1IPTYmFVYg130_assertion; np:hasProvenance dgn-np:NP56255.RAAEEDEH-AVC3Uq8Rb5d-eRE1sWWxzR11eb1IPTYmFVYg130_provenance; np:hasPublicationInfo dgn-np:NP56255.RAAEEDEH-AVC3Uq8Rb5d-eRE1sWWxzR11eb1IPTYmFVYg130_publicationInfo; a np:Nanopublication . dgn-np:NP56255.RAAEEDEH-AVC3Uq8Rb5d-eRE1sWWxzR11eb1IPTYmFVYg130_assertion a np:Assertion . dgn-np:NP56255.RAAEEDEH-AVC3Uq8Rb5d-eRE1sWWxzR11eb1IPTYmFVYg130_provenance a np:Provenance . dgn-np:NP56255.RAAEEDEH-AVC3Uq8Rb5d-eRE1sWWxzR11eb1IPTYmFVYg130_publicationInfo a np:PublicationInfo . } dgn-np:NP56255.RAAEEDEH-AVC3Uq8Rb5d-eRE1sWWxzR11eb1IPTYmFVYg130_assertion { miriam-gene:1393 a ncit:C16612 . lld:C1269683 a ncit:C7057 . dgn-gda:DGN08f2e3aa8f88587822e2a7175b92d911 sio:SIO_000628 miriam-gene:1393, lld:C1269683; a sio:SIO_001122 . } dgn-np:NP56255.RAAEEDEH-AVC3Uq8Rb5d-eRE1sWWxzR11eb1IPTYmFVYg130_provenance { dgn-np:NP56255.RAAEEDEH-AVC3Uq8Rb5d-eRE1sWWxzR11eb1IPTYmFVYg130_assertion dcterms:description "[this study does not provide confirmatory evidence for a role of the CRF-BP gene in the vulnerability for MDD in general. The association between genetic CRF-BP variants and MDD may be sexually dimorphic, but this issue requires further investigation in a ]. 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:17599466; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP56255.RAAEEDEH-AVC3Uq8Rb5d-eRE1sWWxzR11eb1IPTYmFVYg130_publicationInfo { this: dcterms:created "2015-08-25T14:38:10+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X, orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654; pav:createdBy orcid:0000-0003-0169-8159; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }