@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP486126.RA5jY_F0bUuyer20PwKM7F9A4EmX-oLUy_9bstlG9mqog
> .
@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:NP486126.RA5jY_F0bUuyer20PwKM7F9A4EmX-oLUy_9bstlG9mqog130_head
{
this:
np:hasAssertion
dgn-np:NP486126.RA5jY_F0bUuyer20PwKM7F9A4EmX-oLUy_9bstlG9mqog130_assertion
;
np:hasProvenance
dgn-np:NP486126.RA5jY_F0bUuyer20PwKM7F9A4EmX-oLUy_9bstlG9mqog130_provenance
;
np:hasPublicationInfo
dgn-np:NP486126.RA5jY_F0bUuyer20PwKM7F9A4EmX-oLUy_9bstlG9mqog130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP486126.RA5jY_F0bUuyer20PwKM7F9A4EmX-oLUy_9bstlG9mqog130_assertion
a
np:Assertion
.
dgn-np:NP486126.RA5jY_F0bUuyer20PwKM7F9A4EmX-oLUy_9bstlG9mqog130_provenance
a
np:Provenance
.
dgn-np:NP486126.RA5jY_F0bUuyer20PwKM7F9A4EmX-oLUy_9bstlG9mqog130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP486126.RA5jY_F0bUuyer20PwKM7F9A4EmX-oLUy_9bstlG9mqog130_assertion
{
miriam-gene:221477
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGNc2121bb98863b0813090ac3c343928e4
sio:SIO_000628
miriam-gene:221477
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP486126.RA5jY_F0bUuyer20PwKM7F9A4EmX-oLUy_9bstlG9mqog130_provenance
{
dgn-np:NP486126.RA5jY_F0bUuyer20PwKM7F9A4EmX-oLUy_9bstlG9mqog130_assertion
dcterms:description
"[The single nucleotide polymorphism (SNP) rs11066001 of BRAP has been shown to be associated with myocardial infarction (MI), coronary atherosclerosis and carotid atherosclerosis, but it is not clear whether it also plays a role in peripheral artery disease (PAD).]. 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:21301165
;
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:NP486126.RA5jY_F0bUuyer20PwKM7F9A4EmX-oLUy_9bstlG9mqog130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}