@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ> .
@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:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_head {
  this: np:hasAssertion dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_assertion ;
    np:hasProvenance dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_assertion a np:Assertion .
  dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_provenance a np:Provenance .
  dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  lld:C1860224 a ncit:C7057 .
  dgn-gda:DGN6c0b8f0a033dc310fa44120de5ae5cd1 sio:SIO_000628 miriam-gene:4846 , lld:C1860224 ;
    a sio:SIO_001121 .
}
dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_provenance {
  dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_assertion dcterms:description "[We tested the hypothesis that haplotypes, as determined by tagSNPs, in NOS3 would be differentially represented in individuals with and without AMS sampled at the Janai Purnima Festival at Lake Gosain Kunda, Nepal, at 4380 m. Seven SNPs were tested, and a highly significant association (p = 0.004) was found for genotypes of the commonly studied missense polymorphism Glu298Asp (rs 1799983; G/T transversion at base 894).]. 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:19775216 ;
    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:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:54+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" .
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}