@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP471265.RA6hdxtrpFe35323I22Dt7fKcOJw1h2_OazyRxZ8SrZNA> .
@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:NP471265.RA6hdxtrpFe35323I22Dt7fKcOJw1h2_OazyRxZ8SrZNA130_head {
   this: np:hasAssertion dgn-np:NP471265.RA6hdxtrpFe35323I22Dt7fKcOJw1h2_OazyRxZ8SrZNA130_assertion ;
    np:hasProvenance dgn-np:NP471265.RA6hdxtrpFe35323I22Dt7fKcOJw1h2_OazyRxZ8SrZNA130_provenance ;
    np:hasPublicationInfo dgn-np:NP471265.RA6hdxtrpFe35323I22Dt7fKcOJw1h2_OazyRxZ8SrZNA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP471265.RA6hdxtrpFe35323I22Dt7fKcOJw1h2_OazyRxZ8SrZNA130_assertion a np:Assertion .
  dgn-np:NP471265.RA6hdxtrpFe35323I22Dt7fKcOJw1h2_OazyRxZ8SrZNA130_provenance a np:Provenance .
  dgn-np:NP471265.RA6hdxtrpFe35323I22Dt7fKcOJw1h2_OazyRxZ8SrZNA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP471265.RA6hdxtrpFe35323I22Dt7fKcOJw1h2_OazyRxZ8SrZNA130_assertion {
   miriam-gene:414 a ncit:C16612 .
  lld:C0004352 a ncit:C7057 .
  dgn-gda:DGN9cd75dbc1d8a1b90ed29436e954d9aa1 sio:SIO_000628 miriam-gene:414 , lld:C0004352 ;
    a sio:SIO_001121 .
}
dgn-np:NP471265.RA6hdxtrpFe35323I22Dt7fKcOJw1h2_OazyRxZ8SrZNA130_provenance {
   dgn-np:NP471265.RA6hdxtrpFe35323I22Dt7fKcOJw1h2_OazyRxZ8SrZNA130_assertion dcterms:description "[The availability of large and comprehensive registries that include detailed phenotype and genetic information for individuals affected with an ASD and family members is crucial for the discovery of autism susceptibility genes and the development and application of biologically based approaches to diagnosis and treatment.]. 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:20955925 ;
    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:NP471265.RA6hdxtrpFe35323I22Dt7fKcOJw1h2_OazyRxZ8SrZNA130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:42+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" .
}