@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:NP611905.RA6UjHS-rEA7s5JbeedF4KrzYerNjyz7sHPavnw05Yv3Y130_head { this: np:hasAssertion dgn-np:NP611905.RA6UjHS-rEA7s5JbeedF4KrzYerNjyz7sHPavnw05Yv3Y130_assertion; np:hasProvenance dgn-np:NP611905.RA6UjHS-rEA7s5JbeedF4KrzYerNjyz7sHPavnw05Yv3Y130_provenance; np:hasPublicationInfo dgn-np:NP611905.RA6UjHS-rEA7s5JbeedF4KrzYerNjyz7sHPavnw05Yv3Y130_publicationInfo; a np:Nanopublication . dgn-np:NP611905.RA6UjHS-rEA7s5JbeedF4KrzYerNjyz7sHPavnw05Yv3Y130_assertion a np:Assertion . dgn-np:NP611905.RA6UjHS-rEA7s5JbeedF4KrzYerNjyz7sHPavnw05Yv3Y130_provenance a np:Provenance . dgn-np:NP611905.RA6UjHS-rEA7s5JbeedF4KrzYerNjyz7sHPavnw05Yv3Y130_publicationInfo a np:PublicationInfo . } dgn-np:NP611905.RA6UjHS-rEA7s5JbeedF4KrzYerNjyz7sHPavnw05Yv3Y130_assertion { miriam-gene:6392 a ncit:C16612 . lld:C0031511 a ncit:C7057 . dgn-gda:DGN28d4bfefdea7496898c459a2a3a5461c sio:SIO_000628 miriam-gene:6392, lld:C0031511; a sio:SIO_001121 . } dgn-np:NP611905.RA6UjHS-rEA7s5JbeedF4KrzYerNjyz7sHPavnw05Yv3Y130_provenance { dgn-np:NP611905.RA6UjHS-rEA7s5JbeedF4KrzYerNjyz7sHPavnw05Yv3Y130_assertion dcterms:description "[Based on the fact that mutation frequency of the SDHD gene is less than that of allelic loss at chromosome11q, where the SDHD gene is located, this region may contain other candidate tumor-suppressor genes involved in pathogenesis of PCC/PGL.]. 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:17526943; 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:NP611905.RA6UjHS-rEA7s5JbeedF4KrzYerNjyz7sHPavnw05Yv3Y130_publicationInfo { this: dcterms:created "2016-05-13T12:46:23+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" . }