@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE> .
@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/v4.0.0/void/> .

dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_head {
  this: np:hasAssertion dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_assertion;
    np:hasProvenance dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_provenance;
    np:hasPublicationInfo dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_assertion a np:Assertion .
  
  dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_provenance a np:Provenance .
  
  dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_assertion {
  miriam-gene:3845 a ncit:C16612 .
  
  lld:C0587248 a ncit:C7057 .
  
  dgn-gda:DGN5e03417ee6240bab2fdd06a7f919f100 sio:SIO_000628 miriam-gene:3845, lld:C0587248;
    a sio:SIO_001121 .
}

dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_provenance {
  dgn-np:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_assertion dcterms:description
      "[In conclusion, our data underscore the important role of RAS in the pathogenesis of the group of related disorders including NS, CFCS, and CS, and provide clues to the high phenotypic variability of patients with germline KRAS mutations.]. 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:20949621;
    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:NP845909.RAX8dHeWa3pbuSnsfmYw6AzPsJslL1z30rlOL9OaIIhhE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:08+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}