@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP301336.RABXVHo2M7Ecgq1mixYSQdq4NiPaNFfLRGDANYjh9iMR0> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP301336.RABXVHo2M7Ecgq1mixYSQdq4NiPaNFfLRGDANYjh9iMR0130_head {
  this: np:hasAssertion dgn-np:NP301336.RABXVHo2M7Ecgq1mixYSQdq4NiPaNFfLRGDANYjh9iMR0130_assertion;
    np:hasProvenance dgn-np:NP301336.RABXVHo2M7Ecgq1mixYSQdq4NiPaNFfLRGDANYjh9iMR0130_provenance;
    np:hasPublicationInfo dgn-np:NP301336.RABXVHo2M7Ecgq1mixYSQdq4NiPaNFfLRGDANYjh9iMR0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP301336.RABXVHo2M7Ecgq1mixYSQdq4NiPaNFfLRGDANYjh9iMR0130_assertion a np:Assertion .
  
  dgn-np:NP301336.RABXVHo2M7Ecgq1mixYSQdq4NiPaNFfLRGDANYjh9iMR0130_provenance a np:Provenance .
  
  dgn-np:NP301336.RABXVHo2M7Ecgq1mixYSQdq4NiPaNFfLRGDANYjh9iMR0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP301336.RABXVHo2M7Ecgq1mixYSQdq4NiPaNFfLRGDANYjh9iMR0130_assertion {
  miriam-gene:1019 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGNe1ee41aee87033cc0b1c412b724bb835 sio:SIO_000628 miriam-gene:1019, lld:C0027651;
    a sio:SIO_001121 .
}

dgn-np:NP301336.RABXVHo2M7Ecgq1mixYSQdq4NiPaNFfLRGDANYjh9iMR0130_provenance {
  dgn-np:NP301336.RABXVHo2M7Ecgq1mixYSQdq4NiPaNFfLRGDANYjh9iMR0130_assertion dcterms:description
      "[No mobility shifts indicating sequence alterations were observed in 273 tumors and 49 cell lines from diverse kinds of tumors These results suggest that in contrast to melanoma, in many other types of human neoplasms the mutation of the CDK4 gene is very rare.]. 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:12731669;
    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:NP301336.RABXVHo2M7Ecgq1mixYSQdq4NiPaNFfLRGDANYjh9iMR0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:33+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}