@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP218637.RAZXQBkDqJ0-jTWxBHwjrS7RT5lofz2vh7ntvRCY1LOxQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP218637.RAZXQBkDqJ0-jTWxBHwjrS7RT5lofz2vh7ntvRCY1LOxQ130_head
{
this:
np:hasAssertion
dgn-np:NP218637.RAZXQBkDqJ0-jTWxBHwjrS7RT5lofz2vh7ntvRCY1LOxQ130_assertion
;
np:hasProvenance
dgn-np:NP218637.RAZXQBkDqJ0-jTWxBHwjrS7RT5lofz2vh7ntvRCY1LOxQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP218637.RAZXQBkDqJ0-jTWxBHwjrS7RT5lofz2vh7ntvRCY1LOxQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP218637.RAZXQBkDqJ0-jTWxBHwjrS7RT5lofz2vh7ntvRCY1LOxQ130_assertion
a
np:Assertion
.
dgn-np:NP218637.RAZXQBkDqJ0-jTWxBHwjrS7RT5lofz2vh7ntvRCY1LOxQ130_provenance
a
np:Provenance
.
dgn-np:NP218637.RAZXQBkDqJ0-jTWxBHwjrS7RT5lofz2vh7ntvRCY1LOxQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP218637.RAZXQBkDqJ0-jTWxBHwjrS7RT5lofz2vh7ntvRCY1LOxQ130_assertion
{
miriam-gene:19
a
ncit:C16612
.
lld:C3272363
a
ncit:C7057
.
dgn-gda:DGNfdfe94ea72ee390b2ddf319d4d41a9ca
sio:SIO_000628
miriam-gene:19
,
lld:C3272363
;
a
sio:SIO_001122
.
}
dgn-np:NP218637.RAZXQBkDqJ0-jTWxBHwjrS7RT5lofz2vh7ntvRCY1LOxQ130_provenance
{
dgn-np:NP218637.RAZXQBkDqJ0-jTWxBHwjrS7RT5lofz2vh7ntvRCY1LOxQ130_assertion
dcterms:description
"[We investigated 244 unrelated, consecutively enrolled patients with ischemic stroke, 150 patients with coronary heart disease (CHD) and 193 blood donors for allele frequencies (AFs) of three common ABCA1 polymorphisms (R219K, V771M and I883M).]. 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:16446539
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP218637.RAZXQBkDqJ0-jTWxBHwjrS7RT5lofz2vh7ntvRCY1LOxQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:44+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}