@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8> .
@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:NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_head {
   this: np:hasAssertion dgn-np:NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_assertion ;
    np:hasProvenance dgn-np:NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_provenance ;
    np:hasPublicationInfo dgn-np:NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_assertion a np:Assertion .
  dgn-np:NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_provenance a np:Provenance .
  dgn-np:NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_assertion {
   miriam-gene:40 a ncit:C16612 .
  lld:C0004352 a ncit:C7057 .
  dgn-gda:DGN32acfe9603e039b45ed31a1f773ce821 sio:SIO_000628 miriam-gene:40 , lld:C0004352 ;
    a sio:SIO_001122 .
}
dgn-np:NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_provenance {
   dgn-np:NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_assertion dcterms:description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. 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:17376794 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_publicationInfo {
   this: dcterms:created "2015-08-25T14:38:25+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" .
}