@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP589377.RApO0o7aw3iij8u0uGruXxVC-srkm98pEJWed8z6_0y6c> .
@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:NP589377.RApO0o7aw3iij8u0uGruXxVC-srkm98pEJWed8z6_0y6c130_head {
  this: np:hasAssertion dgn-np:NP589377.RApO0o7aw3iij8u0uGruXxVC-srkm98pEJWed8z6_0y6c130_assertion;
    np:hasProvenance dgn-np:NP589377.RApO0o7aw3iij8u0uGruXxVC-srkm98pEJWed8z6_0y6c130_provenance;
    np:hasPublicationInfo dgn-np:NP589377.RApO0o7aw3iij8u0uGruXxVC-srkm98pEJWed8z6_0y6c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP589377.RApO0o7aw3iij8u0uGruXxVC-srkm98pEJWed8z6_0y6c130_assertion a np:Assertion .
  
  dgn-np:NP589377.RApO0o7aw3iij8u0uGruXxVC-srkm98pEJWed8z6_0y6c130_provenance a np:Provenance .
  
  dgn-np:NP589377.RApO0o7aw3iij8u0uGruXxVC-srkm98pEJWed8z6_0y6c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP589377.RApO0o7aw3iij8u0uGruXxVC-srkm98pEJWed8z6_0y6c130_assertion {
  miriam-gene:5604 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNa8fb3b02be73c98e7377eda025504980 sio:SIO_000628 miriam-gene:5604, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP589377.RApO0o7aw3iij8u0uGruXxVC-srkm98pEJWed8z6_0y6c130_provenance {
  dgn-np:NP589377.RApO0o7aw3iij8u0uGruXxVC-srkm98pEJWed8z6_0y6c130_assertion dcterms:description
      "[By using a next-generation sequencer, we further conducted deep sequencing of the MAP2K1 cDNA among 171 human cancer specimens or cell lines, resulting in the identification of one known (D67N) and four novel (R47Q, R49L, I204T and P306H) mutations within MAP2K1.]. 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:22327936;
    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:NP589377.RApO0o7aw3iij8u0uGruXxVC-srkm98pEJWed8z6_0y6c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:54+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" .
}