@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP664431.RAcjn20Ybumzb-Sqz3qkIAX2kOYPub185WEd3Iv1I47oE> .
@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:NP664431.RAcjn20Ybumzb-Sqz3qkIAX2kOYPub185WEd3Iv1I47oE130_head {
  this: np:hasAssertion dgn-np:NP664431.RAcjn20Ybumzb-Sqz3qkIAX2kOYPub185WEd3Iv1I47oE130_assertion;
    np:hasProvenance dgn-np:NP664431.RAcjn20Ybumzb-Sqz3qkIAX2kOYPub185WEd3Iv1I47oE130_provenance;
    np:hasPublicationInfo dgn-np:NP664431.RAcjn20Ybumzb-Sqz3qkIAX2kOYPub185WEd3Iv1I47oE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP664431.RAcjn20Ybumzb-Sqz3qkIAX2kOYPub185WEd3Iv1I47oE130_assertion a np:Assertion .
  
  dgn-np:NP664431.RAcjn20Ybumzb-Sqz3qkIAX2kOYPub185WEd3Iv1I47oE130_provenance a np:Provenance .
  
  dgn-np:NP664431.RAcjn20Ybumzb-Sqz3qkIAX2kOYPub185WEd3Iv1I47oE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP664431.RAcjn20Ybumzb-Sqz3qkIAX2kOYPub185WEd3Iv1I47oE130_assertion {
  miriam-gene:5894 a ncit:C16612 .
  
  lld:C0028326 a ncit:C7057 .
  
  dgn-gda:DGN2e941fba2e49c1e3e356ee28b8d1e611 sio:SIO_000628 miriam-gene:5894, lld:C0028326;
    a sio:SIO_001121 .
}

dgn-np:NP664431.RAcjn20Ybumzb-Sqz3qkIAX2kOYPub185WEd3Iv1I47oE130_provenance {
  dgn-np:NP664431.RAcjn20Ybumzb-Sqz3qkIAX2kOYPub185WEd3Iv1I47oE130_assertion dcterms:description
      "[Germline mutations in genes encoding small GTPases of the RAS family (KRAS and NRAS), modulators of RAS function (PTPN11, SOS1 and SHOC2) or downstream signal transducers (RAF1) are causative for NS.]. 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:20673819;
    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:NP664431.RAcjn20Ybumzb-Sqz3qkIAX2kOYPub185WEd3Iv1I47oE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:19+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" .
}