@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP311556.RAo_O-uQxpQQa_-IECUdJuvZi94C_Sbkt_H4EhEd__PRk> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP311556.RAo_O-uQxpQQa_-IECUdJuvZi94C_Sbkt_H4EhEd__PRk130_head {
  this: np:hasAssertion dgn-np:NP311556.RAo_O-uQxpQQa_-IECUdJuvZi94C_Sbkt_H4EhEd__PRk130_assertion;
    np:hasProvenance dgn-np:NP311556.RAo_O-uQxpQQa_-IECUdJuvZi94C_Sbkt_H4EhEd__PRk130_provenance;
    np:hasPublicationInfo dgn-np:NP311556.RAo_O-uQxpQQa_-IECUdJuvZi94C_Sbkt_H4EhEd__PRk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP311556.RAo_O-uQxpQQa_-IECUdJuvZi94C_Sbkt_H4EhEd__PRk130_assertion a np:Assertion .
  
  dgn-np:NP311556.RAo_O-uQxpQQa_-IECUdJuvZi94C_Sbkt_H4EhEd__PRk130_provenance a np:Provenance .
  
  dgn-np:NP311556.RAo_O-uQxpQQa_-IECUdJuvZi94C_Sbkt_H4EhEd__PRk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP311556.RAo_O-uQxpQQa_-IECUdJuvZi94C_Sbkt_H4EhEd__PRk130_assertion {
  miriam-gene:22882 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN2446d553c207d28ec1fc68f40ec4ea0d sio:SIO_000628 miriam-gene:22882, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP311556.RAo_O-uQxpQQa_-IECUdJuvZi94C_Sbkt_H4EhEd__PRk130_provenance {
  dgn-np:NP311556.RAo_O-uQxpQQa_-IECUdJuvZi94C_Sbkt_H4EhEd__PRk130_assertion dcterms:description
      "[An example is RAS, which is frequently mutated in cancer and contributes to initiation and maintenance of the disease by constitutive signal transduction through protein interaction with effector proteins, like PI3K, RAF and RALGDS.]. 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:17568777;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP311556.RAo_O-uQxpQQa_-IECUdJuvZi94C_Sbkt_H4EhEd__PRk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:58+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}