@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:NP971723.RAlSMF-sN9-CR_NcmU4Qjf4h7Q3IqvxyPNhEasZFJQsqE130_head { this: np:hasAssertion dgn-np:NP971723.RAlSMF-sN9-CR_NcmU4Qjf4h7Q3IqvxyPNhEasZFJQsqE130_assertion; np:hasProvenance dgn-np:NP971723.RAlSMF-sN9-CR_NcmU4Qjf4h7Q3IqvxyPNhEasZFJQsqE130_provenance; np:hasPublicationInfo dgn-np:NP971723.RAlSMF-sN9-CR_NcmU4Qjf4h7Q3IqvxyPNhEasZFJQsqE130_publicationInfo; a np:Nanopublication . dgn-np:NP971723.RAlSMF-sN9-CR_NcmU4Qjf4h7Q3IqvxyPNhEasZFJQsqE130_assertion a np:Assertion . dgn-np:NP971723.RAlSMF-sN9-CR_NcmU4Qjf4h7Q3IqvxyPNhEasZFJQsqE130_provenance a np:Provenance . dgn-np:NP971723.RAlSMF-sN9-CR_NcmU4Qjf4h7Q3IqvxyPNhEasZFJQsqE130_publicationInfo a np:PublicationInfo . } dgn-np:NP971723.RAlSMF-sN9-CR_NcmU4Qjf4h7Q3IqvxyPNhEasZFJQsqE130_assertion { miriam-gene:89884 a ncit:C16612 . lld:C0032002 a ncit:C7057 . dgn-gda:DGN20546cadf44f2ba840c5f650c4d71747 sio:SIO_000628 miriam-gene:89884, lld:C0032002; a sio:SIO_001121 . } dgn-np:NP971723.RAlSMF-sN9-CR_NcmU4Qjf4h7Q3IqvxyPNhEasZFJQsqE130_provenance { dgn-np:NP971723.RAlSMF-sN9-CR_NcmU4Qjf4h7Q3IqvxyPNhEasZFJQsqE130_assertion dcterms:description "[PROK2 and PROKR2 and all genes previously known to be involved in hypopituitarism with pituitary stalk interruption (LHX4, HESX1, OTX2, and SOX3) were screened in 72 index cases with pituitary stalk interruption syndrome from the GENHYPOPIT database.]. 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:22466334; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP971723.RAlSMF-sN9-CR_NcmU4Qjf4h7Q3IqvxyPNhEasZFJQsqE130_publicationInfo { this: dcterms:created "2016-05-13T12:49:05+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }