@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP575613.RAI7325ixbQ8cANPWLxn5L0d1QdaPwMclulTVgsl6NDgM> .
@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:NP575613.RAI7325ixbQ8cANPWLxn5L0d1QdaPwMclulTVgsl6NDgM130_head {
  this: np:hasAssertion dgn-np:NP575613.RAI7325ixbQ8cANPWLxn5L0d1QdaPwMclulTVgsl6NDgM130_assertion;
    np:hasProvenance dgn-np:NP575613.RAI7325ixbQ8cANPWLxn5L0d1QdaPwMclulTVgsl6NDgM130_provenance;
    np:hasPublicationInfo dgn-np:NP575613.RAI7325ixbQ8cANPWLxn5L0d1QdaPwMclulTVgsl6NDgM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP575613.RAI7325ixbQ8cANPWLxn5L0d1QdaPwMclulTVgsl6NDgM130_assertion a np:Assertion .
  
  dgn-np:NP575613.RAI7325ixbQ8cANPWLxn5L0d1QdaPwMclulTVgsl6NDgM130_provenance a np:Provenance .
  
  dgn-np:NP575613.RAI7325ixbQ8cANPWLxn5L0d1QdaPwMclulTVgsl6NDgM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP575613.RAI7325ixbQ8cANPWLxn5L0d1QdaPwMclulTVgsl6NDgM130_assertion {
  miriam-gene:5781 a ncit:C16612 .
  
  lld:C0028326 a ncit:C7057 .
  
  dgn-gda:DGN74e4b214f552502018de37a4c27fdfe3 sio:SIO_000628 miriam-gene:5781, lld:C0028326;
    a sio:SIO_001121 .
}

dgn-np:NP575613.RAI7325ixbQ8cANPWLxn5L0d1QdaPwMclulTVgsl6NDgM130_provenance {
  dgn-np:NP575613.RAI7325ixbQ8cANPWLxn5L0d1QdaPwMclulTVgsl6NDgM130_assertion dcterms:description
      "[We further defined the phenotypic spectrum associated with KRAS missense mutations and provided the first evidence of clinical differences in patients with KRAS mutations compared with Noonan syndrome affected individuals with heterozygous PTPN11 mutations and CFC patients carrying a BRAF, MEK1 or MEK1 alteration, respectively.]. 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:17056636;
    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:NP575613.RAI7325ixbQ8cANPWLxn5L0d1QdaPwMclulTVgsl6NDgM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:06+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" .
}