@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:NP422178.RA2ZeP7VABU9UBI09hbhzDYLLuB8brZO3RkkBjN6YMc10130_head { this: np:hasAssertion dgn-np:NP422178.RA2ZeP7VABU9UBI09hbhzDYLLuB8brZO3RkkBjN6YMc10130_assertion; np:hasProvenance dgn-np:NP422178.RA2ZeP7VABU9UBI09hbhzDYLLuB8brZO3RkkBjN6YMc10130_provenance; np:hasPublicationInfo dgn-np:NP422178.RA2ZeP7VABU9UBI09hbhzDYLLuB8brZO3RkkBjN6YMc10130_publicationInfo; a np:Nanopublication . dgn-np:NP422178.RA2ZeP7VABU9UBI09hbhzDYLLuB8brZO3RkkBjN6YMc10130_assertion a np:Assertion . dgn-np:NP422178.RA2ZeP7VABU9UBI09hbhzDYLLuB8brZO3RkkBjN6YMc10130_provenance a np:Provenance . dgn-np:NP422178.RA2ZeP7VABU9UBI09hbhzDYLLuB8brZO3RkkBjN6YMc10130_publicationInfo a np:PublicationInfo . } dgn-np:NP422178.RA2ZeP7VABU9UBI09hbhzDYLLuB8brZO3RkkBjN6YMc10130_assertion { miriam-gene:2661 a ncit:C16612 . lld:C0025322 a ncit:C7057 . dgn-gda:DGN64642a0de87836ab841b86d7c3abd8af sio:SIO_000628 miriam-gene:2661, lld:C0025322; a sio:SIO_001121 . } dgn-np:NP422178.RA2ZeP7VABU9UBI09hbhzDYLLuB8brZO3RkkBjN6YMc10130_provenance { dgn-np:NP422178.RA2ZeP7VABU9UBI09hbhzDYLLuB8brZO3RkkBjN6YMc10130_assertion dcterms:description "[This case-control study was designed for mutational analysis of the GDF9 coding region in a cohort of women with premature ovarian failure (n = 127), primary amenorrhea (n = 58), and secondary amenorrhea (n = 10) compared with controls (n = 220).]. 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:16278619; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP422178.RA2ZeP7VABU9UBI09hbhzDYLLuB8brZO3RkkBjN6YMc10130_publicationInfo { this: dcterms:created "2015-08-25T14:41:45+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }