@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP742398.RA7Ov7GtjSnTlWLEkGHGGxrvTfeDQGG4VCO7ZHRjFLs-c> .
@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:NP742398.RA7Ov7GtjSnTlWLEkGHGGxrvTfeDQGG4VCO7ZHRjFLs-c130_head {
   this: np:hasAssertion dgn-np:NP742398.RA7Ov7GtjSnTlWLEkGHGGxrvTfeDQGG4VCO7ZHRjFLs-c130_assertion ;
    np:hasProvenance dgn-np:NP742398.RA7Ov7GtjSnTlWLEkGHGGxrvTfeDQGG4VCO7ZHRjFLs-c130_provenance ;
    np:hasPublicationInfo dgn-np:NP742398.RA7Ov7GtjSnTlWLEkGHGGxrvTfeDQGG4VCO7ZHRjFLs-c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP742398.RA7Ov7GtjSnTlWLEkGHGGxrvTfeDQGG4VCO7ZHRjFLs-c130_assertion a np:Assertion .
  dgn-np:NP742398.RA7Ov7GtjSnTlWLEkGHGGxrvTfeDQGG4VCO7ZHRjFLs-c130_provenance a np:Provenance .
  dgn-np:NP742398.RA7Ov7GtjSnTlWLEkGHGGxrvTfeDQGG4VCO7ZHRjFLs-c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP742398.RA7Ov7GtjSnTlWLEkGHGGxrvTfeDQGG4VCO7ZHRjFLs-c130_assertion {
   miriam-gene:4524 a ncit:C16612 .
  lld:C0041107 a ncit:C7057 .
  dgn-gda:DGN94a29f1bb753b585f37e89498ccb2162 sio:SIO_000628 miriam-gene:4524 , lld:C0041107 ;
    a sio:SIO_001121 .
}
dgn-np:NP742398.RA7Ov7GtjSnTlWLEkGHGGxrvTfeDQGG4VCO7ZHRjFLs-c130_provenance {
   dgn-np:NP742398.RA7Ov7GtjSnTlWLEkGHGGxrvTfeDQGG4VCO7ZHRjFLs-c130_assertion dcterms:description "[We analyzed maternal polymorphisms at MTHFR and MTRR in 93 cases of sex-chromosome trisomy, 44 cases of trisomy 18, and 158 cases of autosomal trisomies 2, 7, 10, 13, 14, 15, 16, 18, or 22, and compared the distributions of genotypes to those of control populations.]. 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:11443546 ;
    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:NP742398.RA7Ov7GtjSnTlWLEkGHGGxrvTfeDQGG4VCO7ZHRjFLs-c130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:30+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" .
}