@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP873810.RA9tEaFN1gYlYGSvXytYvc9BbTX2xnuDvNeBVepXE720k> .
@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:NP873810.RA9tEaFN1gYlYGSvXytYvc9BbTX2xnuDvNeBVepXE720k130_head {
  this: np:hasAssertion dgn-np:NP873810.RA9tEaFN1gYlYGSvXytYvc9BbTX2xnuDvNeBVepXE720k130_assertion;
    np:hasProvenance dgn-np:NP873810.RA9tEaFN1gYlYGSvXytYvc9BbTX2xnuDvNeBVepXE720k130_provenance;
    np:hasPublicationInfo dgn-np:NP873810.RA9tEaFN1gYlYGSvXytYvc9BbTX2xnuDvNeBVepXE720k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP873810.RA9tEaFN1gYlYGSvXytYvc9BbTX2xnuDvNeBVepXE720k130_assertion a np:Assertion .
  
  dgn-np:NP873810.RA9tEaFN1gYlYGSvXytYvc9BbTX2xnuDvNeBVepXE720k130_provenance a np:Provenance .
  
  dgn-np:NP873810.RA9tEaFN1gYlYGSvXytYvc9BbTX2xnuDvNeBVepXE720k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP873810.RA9tEaFN1gYlYGSvXytYvc9BbTX2xnuDvNeBVepXE720k130_assertion {
  miriam-gene:8731 a ncit:C16612 .
  
  lld:C0001614 a ncit:C7057 .
  
  dgn-gda:DGNd7ee38a93e75cf34c79a7f1f9c6509ed sio:SIO_000628 miriam-gene:8731, lld:C0001614;
    a sio:SIO_001121 .
}

dgn-np:NP873810.RA9tEaFN1gYlYGSvXytYvc9BbTX2xnuDvNeBVepXE720k130_provenance {
  dgn-np:NP873810.RA9tEaFN1gYlYGSvXytYvc9BbTX2xnuDvNeBVepXE720k130_assertion dcterms:description
      "[A functional variant in the promoter of the gene encoding the MET receptor tyrosine kinase is associated with autism spectrum disorder, and MET protein expression is decreased in the temporal cortex of subjects with autism spectrum disorder.]. 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:19255034;
    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:NP873810.RA9tEaFN1gYlYGSvXytYvc9BbTX2xnuDvNeBVepXE720k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:54+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" .
}