@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:NP303512.RA4buZz6WaG7At8Yw2i_cUT9hf_5m92eAF6BjvW5WKL0E130_head { this: np:hasAssertion dgn-np:NP303512.RA4buZz6WaG7At8Yw2i_cUT9hf_5m92eAF6BjvW5WKL0E130_assertion; np:hasProvenance dgn-np:NP303512.RA4buZz6WaG7At8Yw2i_cUT9hf_5m92eAF6BjvW5WKL0E130_provenance; np:hasPublicationInfo dgn-np:NP303512.RA4buZz6WaG7At8Yw2i_cUT9hf_5m92eAF6BjvW5WKL0E130_publicationInfo; a np:Nanopublication . dgn-np:NP303512.RA4buZz6WaG7At8Yw2i_cUT9hf_5m92eAF6BjvW5WKL0E130_assertion a np:Assertion . dgn-np:NP303512.RA4buZz6WaG7At8Yw2i_cUT9hf_5m92eAF6BjvW5WKL0E130_provenance a np:Provenance . dgn-np:NP303512.RA4buZz6WaG7At8Yw2i_cUT9hf_5m92eAF6BjvW5WKL0E130_publicationInfo a np:PublicationInfo . } dgn-np:NP303512.RA4buZz6WaG7At8Yw2i_cUT9hf_5m92eAF6BjvW5WKL0E130_assertion { miriam-gene:1027 a ncit:C16612 . lld:C0238339 a ncit:C7057 . dgn-gda:DGN6dea077ea2bdda3456db9bd6bacf15ce sio:SIO_000628 miriam-gene:1027, lld:C0238339; a sio:SIO_001121 . } dgn-np:NP303512.RA4buZz6WaG7At8Yw2i_cUT9hf_5m92eAF6BjvW5WKL0E130_provenance { dgn-np:NP303512.RA4buZz6WaG7At8Yw2i_cUT9hf_5m92eAF6BjvW5WKL0E130_assertion dcterms:description "[In light of the evidence for linkage between the chromosomal location of the CDKN1B gene (12p13) and prostate cancer susceptibility in several hereditary prostate cancer (HPC) populations, we hypothesized that sequence variants of CDKN1B play a role in HPC.]. 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:15026335; 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:NP303512.RA4buZz6WaG7At8Yw2i_cUT9hf_5m92eAF6BjvW5WKL0E130_publicationInfo { this: dcterms:created "2015-08-25T14:40:34+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" . }