@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP259040.RAsCrUt1Il3s3hgnk3vPDi7RBSRdbU5Sv3XbdOgWb99Pc> .
@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:NP259040.RAsCrUt1Il3s3hgnk3vPDi7RBSRdbU5Sv3XbdOgWb99Pc130_head {
  this: np:hasAssertion dgn-np:NP259040.RAsCrUt1Il3s3hgnk3vPDi7RBSRdbU5Sv3XbdOgWb99Pc130_assertion;
    np:hasProvenance dgn-np:NP259040.RAsCrUt1Il3s3hgnk3vPDi7RBSRdbU5Sv3XbdOgWb99Pc130_provenance;
    np:hasPublicationInfo dgn-np:NP259040.RAsCrUt1Il3s3hgnk3vPDi7RBSRdbU5Sv3XbdOgWb99Pc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP259040.RAsCrUt1Il3s3hgnk3vPDi7RBSRdbU5Sv3XbdOgWb99Pc130_assertion a np:Assertion .
  
  dgn-np:NP259040.RAsCrUt1Il3s3hgnk3vPDi7RBSRdbU5Sv3XbdOgWb99Pc130_provenance a np:Provenance .
  
  dgn-np:NP259040.RAsCrUt1Il3s3hgnk3vPDi7RBSRdbU5Sv3XbdOgWb99Pc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP259040.RAsCrUt1Il3s3hgnk3vPDi7RBSRdbU5Sv3XbdOgWb99Pc130_assertion {
  miriam-gene:4204 a ncit:C16612 .
  
  lld:C1510586 a ncit:C7057 .
  
  dgn-gda:DGNb144b062e8c94ba54537dee85e299b07 sio:SIO_000628 miriam-gene:4204, lld:C1510586;
    a sio:SIO_001121 .
}

dgn-np:NP259040.RAsCrUt1Il3s3hgnk3vPDi7RBSRdbU5Sv3XbdOgWb99Pc130_provenance {
  dgn-np:NP259040.RAsCrUt1Il3s3hgnk3vPDi7RBSRdbU5Sv3XbdOgWb99Pc130_assertion dcterms:description
      "[Analysis of polymorphic markers spanning the gene and comprising both microsatellites and single nucleotide polymorphisms (SNPs) by the transmission disequilibrium test in two collections of families (219 in total), one in the USA and one in the UK, has provided evidence for significant association (P = 0.009) for a three-marker SNP haplotype of MECP2 with autism/autism spectrum disorders.]. 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:19125863;
    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:NP259040.RAsCrUt1Il3s3hgnk3vPDi7RBSRdbU5Sv3XbdOgWb99Pc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:24+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" .
}