@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:NP1414522.RAiff8GJ9yW06nQXc6aOzEjqWLxDxqZSSm0vR0zkx9b6U130_head { this: np:hasAssertion dgn-np:NP1414522.RAiff8GJ9yW06nQXc6aOzEjqWLxDxqZSSm0vR0zkx9b6U130_assertion; np:hasProvenance dgn-np:NP1414522.RAiff8GJ9yW06nQXc6aOzEjqWLxDxqZSSm0vR0zkx9b6U130_provenance; np:hasPublicationInfo dgn-np:NP1414522.RAiff8GJ9yW06nQXc6aOzEjqWLxDxqZSSm0vR0zkx9b6U130_publicationInfo; a np:Nanopublication . dgn-np:NP1414522.RAiff8GJ9yW06nQXc6aOzEjqWLxDxqZSSm0vR0zkx9b6U130_assertion a np:Assertion . dgn-np:NP1414522.RAiff8GJ9yW06nQXc6aOzEjqWLxDxqZSSm0vR0zkx9b6U130_provenance a np:Provenance . dgn-np:NP1414522.RAiff8GJ9yW06nQXc6aOzEjqWLxDxqZSSm0vR0zkx9b6U130_publicationInfo a np:PublicationInfo . } dgn-np:NP1414522.RAiff8GJ9yW06nQXc6aOzEjqWLxDxqZSSm0vR0zkx9b6U130_assertion { miriam-gene:1030 a ncit:C16612 . lld:C0025202 a ncit:C7057 . dgn-gda:DGNba893a97788c18279bd69c0a74a70c75 sio:SIO_000628 miriam-gene:1030, lld:C0025202; a sio:SIO_001121 . } dgn-np:NP1414522.RAiff8GJ9yW06nQXc6aOzEjqWLxDxqZSSm0vR0zkx9b6U130_provenance { dgn-np:NP1414522.RAiff8GJ9yW06nQXc6aOzEjqWLxDxqZSSm0vR0zkx9b6U130_assertion dcterms:description "[In addition, two chromosome 9 derivatives that were microdeleted in the region of the p16INK4A/p15INK4B locus were transferred to determine whether an additional melanoma TSG or TSGs reside on chromosome 9p, as indicated by previous melanoma allele loss studies.]. 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:9973191; 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:NP1414522.RAiff8GJ9yW06nQXc6aOzEjqWLxDxqZSSm0vR0zkx9b6U130_publicationInfo { this: dcterms:created "2016-05-13T12:52:28+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" . }