@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:NP920017.RAAStKrPfN_e5g2U-ssqhWdIuXpHn8cI5_iVGpLFUV6xQ130_head { this: np:hasAssertion dgn-np:NP920017.RAAStKrPfN_e5g2U-ssqhWdIuXpHn8cI5_iVGpLFUV6xQ130_assertion; np:hasProvenance dgn-np:NP920017.RAAStKrPfN_e5g2U-ssqhWdIuXpHn8cI5_iVGpLFUV6xQ130_provenance; np:hasPublicationInfo dgn-np:NP920017.RAAStKrPfN_e5g2U-ssqhWdIuXpHn8cI5_iVGpLFUV6xQ130_publicationInfo; a np:Nanopublication . dgn-np:NP920017.RAAStKrPfN_e5g2U-ssqhWdIuXpHn8cI5_iVGpLFUV6xQ130_assertion a np:Assertion . dgn-np:NP920017.RAAStKrPfN_e5g2U-ssqhWdIuXpHn8cI5_iVGpLFUV6xQ130_provenance a np:Provenance . dgn-np:NP920017.RAAStKrPfN_e5g2U-ssqhWdIuXpHn8cI5_iVGpLFUV6xQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP920017.RAAStKrPfN_e5g2U-ssqhWdIuXpHn8cI5_iVGpLFUV6xQ130_assertion { miriam-gene:55655 a ncit:C16612 . lld:C0376358 a ncit:C7057 . dgn-gda:DGN8f3c98684628407912576e29ad996239 sio:SIO_000628 miriam-gene:55655, lld:C0376358; a sio:SIO_001121 . } dgn-np:NP920017.RAAStKrPfN_e5g2U-ssqhWdIuXpHn8cI5_iVGpLFUV6xQ130_provenance { dgn-np:NP920017.RAAStKrPfN_e5g2U-ssqhWdIuXpHn8cI5_iVGpLFUV6xQ130_assertion dcterms:description "[Our study did not reveal predisposition genes for hereditary prostate cancer as the founder mutations of the BRCA1 and NBS1 genes are rarely detected in Latvia, but showed the importance of evaluation risk individually as a positive family history of cancer was associated with the earlier onset of prostate cancer.]. 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:22186123; 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:NP920017.RAAStKrPfN_e5g2U-ssqhWdIuXpHn8cI5_iVGpLFUV6xQ130_publicationInfo { this: dcterms:created "2015-08-25T14:47:02+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" . }