@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP164077.RAfi0gSv5aqG54XJAyUIQPLRow8YLdEbfhyH_yTOo1Ebs> .
@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:NP164077.RAfi0gSv5aqG54XJAyUIQPLRow8YLdEbfhyH_yTOo1Ebs130_head {
  this: np:hasAssertion dgn-np:NP164077.RAfi0gSv5aqG54XJAyUIQPLRow8YLdEbfhyH_yTOo1Ebs130_assertion ;
    np:hasProvenance dgn-np:NP164077.RAfi0gSv5aqG54XJAyUIQPLRow8YLdEbfhyH_yTOo1Ebs130_provenance ;
    np:hasPublicationInfo dgn-np:NP164077.RAfi0gSv5aqG54XJAyUIQPLRow8YLdEbfhyH_yTOo1Ebs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP164077.RAfi0gSv5aqG54XJAyUIQPLRow8YLdEbfhyH_yTOo1Ebs130_assertion a np:Assertion .
  dgn-np:NP164077.RAfi0gSv5aqG54XJAyUIQPLRow8YLdEbfhyH_yTOo1Ebs130_provenance a np:Provenance .
  dgn-np:NP164077.RAfi0gSv5aqG54XJAyUIQPLRow8YLdEbfhyH_yTOo1Ebs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP164077.RAfi0gSv5aqG54XJAyUIQPLRow8YLdEbfhyH_yTOo1Ebs130_assertion {
  miriam-gene:79811 a ncit:C16612 .
  lld:C0001614 a ncit:C7057 .
  dgn-gda:DGN4013fe1136494e46c04dc7ff003c4b4a sio:SIO_000628 miriam-gene:79811 , lld:C0001614 ;
    a sio:SIO_001121 .
}
dgn-np:NP164077.RAfi0gSv5aqG54XJAyUIQPLRow8YLdEbfhyH_yTOo1Ebs130_provenance {
  dgn-np:NP164077.RAfi0gSv5aqG54XJAyUIQPLRow8YLdEbfhyH_yTOo1Ebs130_assertion dcterms:description "[The MET gene has been regarded as a promising candidate gene for this disorder because it is located within a replicated linkage interval, is involved in pathways affecting the development of the cerebral cortex and cerebellum in ways relevant to autism patients, and has shown significant association signals in previous studies.]. 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:22110649 ;
    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:NP164077.RAfi0gSv5aqG54XJAyUIQPLRow8YLdEbfhyH_yTOo1Ebs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}