@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP925436.RAZUO_Rdg4YHpCipv7nBeMU4wTt0GbRrc_8l49vW4fLzE> .
@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:NP925436.RAZUO_Rdg4YHpCipv7nBeMU4wTt0GbRrc_8l49vW4fLzE130_head {
   this: np:hasAssertion dgn-np:NP925436.RAZUO_Rdg4YHpCipv7nBeMU4wTt0GbRrc_8l49vW4fLzE130_assertion ;
    np:hasProvenance dgn-np:NP925436.RAZUO_Rdg4YHpCipv7nBeMU4wTt0GbRrc_8l49vW4fLzE130_provenance ;
    np:hasPublicationInfo dgn-np:NP925436.RAZUO_Rdg4YHpCipv7nBeMU4wTt0GbRrc_8l49vW4fLzE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP925436.RAZUO_Rdg4YHpCipv7nBeMU4wTt0GbRrc_8l49vW4fLzE130_assertion a np:Assertion .
  dgn-np:NP925436.RAZUO_Rdg4YHpCipv7nBeMU4wTt0GbRrc_8l49vW4fLzE130_provenance a np:Provenance .
  dgn-np:NP925436.RAZUO_Rdg4YHpCipv7nBeMU4wTt0GbRrc_8l49vW4fLzE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP925436.RAZUO_Rdg4YHpCipv7nBeMU4wTt0GbRrc_8l49vW4fLzE130_assertion {
   miriam-gene:4139 a ncit:C16612 .
  lld:C1510586 a ncit:C7057 .
  dgn-gda:DGN3c128622e8867e4aa8501cf704c6ad0f sio:SIO_000628 miriam-gene:4139 , lld:C1510586 ;
    a sio:SIO_001121 .
}
dgn-np:NP925436.RAZUO_Rdg4YHpCipv7nBeMU4wTt0GbRrc_8l49vW4fLzE130_provenance {
   dgn-np:NP925436.RAZUO_Rdg4YHpCipv7nBeMU4wTt0GbRrc_8l49vW4fLzE130_assertion dcterms:description "[High-resolution single-nucleotide polymorphisms (126 SNPs) genotyping across the chromosome 1q41-q42 region, followed by a MARK1 (microtubule affinity-regulating kinase 1)-tagged-SNP association study in 276 families with autism from the Autism Genetic Research Exchange, showed that several SNPs within the MARK1 gene were significantly associated with ASDs by transmission disequilibrium tests.]. 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:18492799 ;
    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:NP925436.RAZUO_Rdg4YHpCipv7nBeMU4wTt0GbRrc_8l49vW4fLzE130_publicationInfo {
   this: dcterms:created "2014-10-02T12:41:27+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" .
}