@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP634118.RAQt0Q3IRN2ZrWWWO8_qhDHfTixloWE_qM-hY18p97t6I
> .
@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:NP634118.RAQt0Q3IRN2ZrWWWO8_qhDHfTixloWE_qM-hY18p97t6I130_head
{
this:
np:hasAssertion
dgn-np:NP634118.RAQt0Q3IRN2ZrWWWO8_qhDHfTixloWE_qM-hY18p97t6I130_assertion
;
np:hasProvenance
dgn-np:NP634118.RAQt0Q3IRN2ZrWWWO8_qhDHfTixloWE_qM-hY18p97t6I130_provenance
;
np:hasPublicationInfo
dgn-np:NP634118.RAQt0Q3IRN2ZrWWWO8_qhDHfTixloWE_qM-hY18p97t6I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP634118.RAQt0Q3IRN2ZrWWWO8_qhDHfTixloWE_qM-hY18p97t6I130_assertion
a
np:Assertion
.
dgn-np:NP634118.RAQt0Q3IRN2ZrWWWO8_qhDHfTixloWE_qM-hY18p97t6I130_provenance
a
np:Provenance
.
dgn-np:NP634118.RAQt0Q3IRN2ZrWWWO8_qhDHfTixloWE_qM-hY18p97t6I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP634118.RAQt0Q3IRN2ZrWWWO8_qhDHfTixloWE_qM-hY18p97t6I130_assertion
{
miriam-gene:3156
a
ncit:C16612
.
lld:C0020443
a
ncit:C7057
.
dgn-gda:DGN52d89092fec4e91e5fd26584709d6adf
sio:SIO_000628
miriam-gene:3156
,
lld:C0020443
;
a
sio:SIO_001121
.
}
dgn-np:NP634118.RAQt0Q3IRN2ZrWWWO8_qhDHfTixloWE_qM-hY18p97t6I130_provenance
{
dgn-np:NP634118.RAQt0Q3IRN2ZrWWWO8_qhDHfTixloWE_qM-hY18p97t6I130_assertion
dcterms:description
"[In this population-based case-control study, the frequencies of -911 C>A polymorphism (rs3761740) of the HMGCR gene in patients with coronary heart disease (CHD) and healthy subjects were investigated and the correlations between the different genotypes and hypercholesterolemia with cardiovascular risk factors were analyzed.]. 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:23933271
;
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:NP634118.RAQt0Q3IRN2ZrWWWO8_qhDHfTixloWE_qM-hY18p97t6I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:22+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" .
}