@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP833324.RAN4JrgP3P1jG30n0yIgo_EIUr09z9UIfy1tPGfpX2H6M> .
@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:NP833324.RAN4JrgP3P1jG30n0yIgo_EIUr09z9UIfy1tPGfpX2H6M130_head {
   this: np:hasAssertion dgn-np:NP833324.RAN4JrgP3P1jG30n0yIgo_EIUr09z9UIfy1tPGfpX2H6M130_assertion ;
    np:hasProvenance dgn-np:NP833324.RAN4JrgP3P1jG30n0yIgo_EIUr09z9UIfy1tPGfpX2H6M130_provenance ;
    np:hasPublicationInfo dgn-np:NP833324.RAN4JrgP3P1jG30n0yIgo_EIUr09z9UIfy1tPGfpX2H6M130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP833324.RAN4JrgP3P1jG30n0yIgo_EIUr09z9UIfy1tPGfpX2H6M130_assertion a np:Assertion .
  dgn-np:NP833324.RAN4JrgP3P1jG30n0yIgo_EIUr09z9UIfy1tPGfpX2H6M130_provenance a np:Provenance .
  dgn-np:NP833324.RAN4JrgP3P1jG30n0yIgo_EIUr09z9UIfy1tPGfpX2H6M130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP833324.RAN4JrgP3P1jG30n0yIgo_EIUr09z9UIfy1tPGfpX2H6M130_assertion {
   miriam-gene:4139 a ncit:C16612 .
  lld:C0004352 a ncit:C7057 .
  dgn-gda:DGN579fa3bb486a172da883a09fc467bff4 sio:SIO_000628 miriam-gene:4139 , lld:C0004352 ;
    a sio:SIO_001121 .
}
dgn-np:NP833324.RAN4JrgP3P1jG30n0yIgo_EIUr09z9UIfy1tPGfpX2H6M130_provenance {
   dgn-np:NP833324.RAN4JrgP3P1jG30n0yIgo_EIUr09z9UIfy1tPGfpX2H6M130_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:NP833324.RAN4JrgP3P1jG30n0yIgo_EIUr09z9UIfy1tPGfpX2H6M130_publicationInfo {
   this: dcterms:created "2014-10-02T12:40:30+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" .
}