@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM
> .
@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:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_head
{
this:
np:hasAssertion
dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_assertion
;
np:hasProvenance
dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_provenance
;
np:hasPublicationInfo
dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_assertion
a
np:Assertion
.
dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_provenance
a
np:Provenance
.
dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_assertion
{
miriam-gene:3949
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNe3a34098f1b9a9da1bbb41b664bb6942
sio:SIO_000628
miriam-gene:3949
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_provenance
{
dgn-np:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_assertion
dcterms:description
"[The possible association of genetic markers at the apolipoprotein E (HhaI polymorphism), apolipoprotein B (XbaI, EcoRI and Ins/Del polymorphisms), and low-density lipoprotein receptor (LDLR) (AvaII, HincII and PvuII polymorphisms) with coronary artery disease (CAD) was evaluated in 50 Brazilian women with CAD diagnosed by angiography and in 100 healthy women (controls).]. 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:10958870
;
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:NP238894.RA6czfkq5_hupMwZs1lxa5xw1_rRDfm6FY9IdHLWYlbIM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}