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> .
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> .
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http://www.w3.org/2001/XMLSchema#
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http://semanticscience.org/resource/
> .
@prefix ncit: <
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http://linkedlifedata.com/resource/umls/id/
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http://identifiers.org/ncbigene/
> .
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http://identifiers.org/pubmed/
> .
@prefix eco: <
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> .
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http://purl.org/ontology/wi/core#
> .
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http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
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http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
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http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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miriam-gene:948
a
ncit:C16612
.
lld:C0020443
a
ncit:C7057
.
dgn-gda:DGN280ef707b16a8eeaa3de5210991cf7ef
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dgn-np:NP530793.RAPlqu6bVI2ISAPay6UEcdtLoctoV-4ie594Hmd4qzEvY130_assertion
dcterms:description
"[Allele and genotype disease association test revealed that APOB rs693 (OR: 2.2 [1.5-3.2], p=0.0001) and CD36 rs1984112 (OR: 3.7 [1.9-7.0], p=0.0002) SNPs were independent risk factors for hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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sio:SIO_000772
miriam-pubmed:23247049
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pav:importedOn
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xsd:date
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dgn-void:source_evidence_literature
a
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rdfs:comment
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rdfs:label
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dgn-np:NP530793.RAPlqu6bVI2ISAPay6UEcdtLoctoV-4ie594Hmd4qzEvY130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
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