@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:NP305712.RAod1hDuNRSP9VVlco7J65BHyn3arkzy9v3Hq4yi5-4BU130_head { this: np:hasAssertion dgn-np:NP305712.RAod1hDuNRSP9VVlco7J65BHyn3arkzy9v3Hq4yi5-4BU130_assertion; np:hasProvenance dgn-np:NP305712.RAod1hDuNRSP9VVlco7J65BHyn3arkzy9v3Hq4yi5-4BU130_provenance; np:hasPublicationInfo dgn-np:NP305712.RAod1hDuNRSP9VVlco7J65BHyn3arkzy9v3Hq4yi5-4BU130_publicationInfo; a np:Nanopublication . dgn-np:NP305712.RAod1hDuNRSP9VVlco7J65BHyn3arkzy9v3Hq4yi5-4BU130_assertion a np:Assertion . dgn-np:NP305712.RAod1hDuNRSP9VVlco7J65BHyn3arkzy9v3Hq4yi5-4BU130_provenance a np:Provenance . dgn-np:NP305712.RAod1hDuNRSP9VVlco7J65BHyn3arkzy9v3Hq4yi5-4BU130_publicationInfo a np:PublicationInfo . } dgn-np:NP305712.RAod1hDuNRSP9VVlco7J65BHyn3arkzy9v3Hq4yi5-4BU130_assertion { miriam-gene:1029 a ncit:C16612 . lld:C0278704 a ncit:C7057 . dgn-gda:DGN737415a8b747d93948e7f6f079e8b2af sio:SIO_000628 miriam-gene:1029, lld:C0278704; a sio:SIO_001121 . } dgn-np:NP305712.RAod1hDuNRSP9VVlco7J65BHyn3arkzy9v3Hq4yi5-4BU130_provenance { dgn-np:NP305712.RAod1hDuNRSP9VVlco7J65BHyn3arkzy9v3Hq4yi5-4BU130_assertion dcterms:description "[By comparison with the other germ line deletions at the CDKN2A, CDKN2B and CDKN2BAS gene cluster reported in melanoma susceptible families, the deletion detected in the two sisters is peculiar for its de novo origin and for its extension, as it represents the largest constitutive deletion at 9p21.3 region identified so far.In addition, the two studied cases add to other evidence indicating association of melanoma with exposure to ionizing radiation and with second neoplasm after childhood 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:24884915; 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:NP305712.RAod1hDuNRSP9VVlco7J65BHyn3arkzy9v3Hq4yi5-4BU130_publicationInfo { this: dcterms:created "2015-08-25T14:40:35+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" . }