@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:NP1005185.RAlU76OsydD8qWAptbVUtP7QqfS4B-5yAqrB1R6zN8UhY130_head { this: np:hasAssertion dgn-np:NP1005185.RAlU76OsydD8qWAptbVUtP7QqfS4B-5yAqrB1R6zN8UhY130_assertion; np:hasProvenance dgn-np:NP1005185.RAlU76OsydD8qWAptbVUtP7QqfS4B-5yAqrB1R6zN8UhY130_provenance; np:hasPublicationInfo dgn-np:NP1005185.RAlU76OsydD8qWAptbVUtP7QqfS4B-5yAqrB1R6zN8UhY130_publicationInfo; a np:Nanopublication . dgn-np:NP1005185.RAlU76OsydD8qWAptbVUtP7QqfS4B-5yAqrB1R6zN8UhY130_assertion a np:Assertion . dgn-np:NP1005185.RAlU76OsydD8qWAptbVUtP7QqfS4B-5yAqrB1R6zN8UhY130_provenance a np:Provenance . dgn-np:NP1005185.RAlU76OsydD8qWAptbVUtP7QqfS4B-5yAqrB1R6zN8UhY130_publicationInfo a np:PublicationInfo . } dgn-np:NP1005185.RAlU76OsydD8qWAptbVUtP7QqfS4B-5yAqrB1R6zN8UhY130_assertion { miriam-gene:595 a ncit:C16612 . lld:C0025202 a ncit:C7057 . dgn-gda:DGN99701e1a24b19ace13d759194c280344 sio:SIO_000628 miriam-gene:595, lld:C0025202; a sio:SIO_001121 . } dgn-np:NP1005185.RAlU76OsydD8qWAptbVUtP7QqfS4B-5yAqrB1R6zN8UhY130_provenance { dgn-np:NP1005185.RAlU76OsydD8qWAptbVUtP7QqfS4B-5yAqrB1R6zN8UhY130_assertion dcterms:description "[Using a four-probe fluorescence in situ hybridization (FISH) assay targeting RREB1, MYB, Cep6, and CCND1, we found that seven of the eight propositus cases showed chromosomal aberrations consistent with the standardized FISH diagnostic criteria for melanoma.]. 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:22892832; 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:NP1005185.RAlU76OsydD8qWAptbVUtP7QqfS4B-5yAqrB1R6zN8UhY130_publicationInfo { this: dcterms:created "2016-05-13T12:49:21+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" . }