@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:NP1367693.RAlkQl8XRYmsj-6vhTm3cK_q6DW_EtjUOBgm2WJ08PLp0130_head { this: np:hasAssertion dgn-np:NP1367693.RAlkQl8XRYmsj-6vhTm3cK_q6DW_EtjUOBgm2WJ08PLp0130_assertion; np:hasProvenance dgn-np:NP1367693.RAlkQl8XRYmsj-6vhTm3cK_q6DW_EtjUOBgm2WJ08PLp0130_provenance; np:hasPublicationInfo dgn-np:NP1367693.RAlkQl8XRYmsj-6vhTm3cK_q6DW_EtjUOBgm2WJ08PLp0130_publicationInfo; a np:Nanopublication . dgn-np:NP1367693.RAlkQl8XRYmsj-6vhTm3cK_q6DW_EtjUOBgm2WJ08PLp0130_assertion a np:Assertion . dgn-np:NP1367693.RAlkQl8XRYmsj-6vhTm3cK_q6DW_EtjUOBgm2WJ08PLp0130_provenance a np:Provenance . dgn-np:NP1367693.RAlkQl8XRYmsj-6vhTm3cK_q6DW_EtjUOBgm2WJ08PLp0130_publicationInfo a np:PublicationInfo . } dgn-np:NP1367693.RAlkQl8XRYmsj-6vhTm3cK_q6DW_EtjUOBgm2WJ08PLp0130_assertion { miriam-gene:6046 a ncit:C16612 . lld:C0032000 a ncit:C7057 . dgn-gda:DGN52af41c83afbe5df92d6562dac26de7c sio:SIO_000628 miriam-gene:6046, lld:C0032000; a sio:SIO_001121 . } dgn-np:NP1367693.RAlkQl8XRYmsj-6vhTm3cK_q6DW_EtjUOBgm2WJ08PLp0130_provenance { dgn-np:NP1367693.RAlkQl8XRYmsj-6vhTm3cK_q6DW_EtjUOBgm2WJ08PLp0130_assertion dcterms:description "[Hyperactivity of the FSH axis caused by activating mutations of the FSH receptor gene might parallel the presentation of FSH secreting pituitary adenomas with Sertoli cell hypertrophy in men (Heseltine et al., 1989) or reversible premature ovarian failure in women (Moses et al., 1986; Okuda et al., 1989).]. 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:9039330; 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:NP1367693.RAlkQl8XRYmsj-6vhTm3cK_q6DW_EtjUOBgm2WJ08PLp0130_publicationInfo { this: dcterms:created "2016-05-13T12:52:06+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" . }