@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP319182.RAD98Ao8mE8QWXIxIlzHcj7EPUvvWQOTdA2XkyFbnpaYE> .
@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:NP319182.RAD98Ao8mE8QWXIxIlzHcj7EPUvvWQOTdA2XkyFbnpaYE130_head {
  this: np:hasAssertion dgn-np:NP319182.RAD98Ao8mE8QWXIxIlzHcj7EPUvvWQOTdA2XkyFbnpaYE130_assertion ;
    np:hasProvenance dgn-np:NP319182.RAD98Ao8mE8QWXIxIlzHcj7EPUvvWQOTdA2XkyFbnpaYE130_provenance ;
    np:hasPublicationInfo dgn-np:NP319182.RAD98Ao8mE8QWXIxIlzHcj7EPUvvWQOTdA2XkyFbnpaYE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP319182.RAD98Ao8mE8QWXIxIlzHcj7EPUvvWQOTdA2XkyFbnpaYE130_assertion a np:Assertion .
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  dgn-np:NP319182.RAD98Ao8mE8QWXIxIlzHcj7EPUvvWQOTdA2XkyFbnpaYE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP319182.RAD98Ao8mE8QWXIxIlzHcj7EPUvvWQOTdA2XkyFbnpaYE130_assertion {
  miriam-gene:1289 a ncit:C16612 .
  lld:C0266539 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP319182.RAD98Ao8mE8QWXIxIlzHcj7EPUvvWQOTdA2XkyFbnpaYE130_provenance {
  dgn-np:NP319182.RAD98Ao8mE8QWXIxIlzHcj7EPUvvWQOTdA2XkyFbnpaYE130_assertion dcterms:description "[We conducted two genome-wide association studies for CCT in 5080 individuals drawn from two ethnic populations in Singapore (2538 Indian and 2542 Malays) and identified novel genetic loci significantly associated with CCT (COL8A2 rs96067, p(meta) = 5.40 × 10⁻¹³, interval of RXRA-COL5A1 rs1536478, p(meta) = 3.05 × 10⁻⁹).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP319182.RAD98Ao8mE8QWXIxIlzHcj7EPUvvWQOTdA2XkyFbnpaYE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:05+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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    dcterms:subject sio:SIO_000983 ;
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    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> ;
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