@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP108503.RAj4cxQQ-4CtuTf_5_CBTeb-6HCZsFGa1K-L9wYOJdCZE
> .
@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:NP108503.RAj4cxQQ-4CtuTf_5_CBTeb-6HCZsFGa1K-L9wYOJdCZE130_head
{
this:
np:hasAssertion
dgn-np:NP108503.RAj4cxQQ-4CtuTf_5_CBTeb-6HCZsFGa1K-L9wYOJdCZE130_assertion
;
np:hasProvenance
dgn-np:NP108503.RAj4cxQQ-4CtuTf_5_CBTeb-6HCZsFGa1K-L9wYOJdCZE130_provenance
;
np:hasPublicationInfo
dgn-np:NP108503.RAj4cxQQ-4CtuTf_5_CBTeb-6HCZsFGa1K-L9wYOJdCZE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP108503.RAj4cxQQ-4CtuTf_5_CBTeb-6HCZsFGa1K-L9wYOJdCZE130_assertion
a
np:Assertion
.
dgn-np:NP108503.RAj4cxQQ-4CtuTf_5_CBTeb-6HCZsFGa1K-L9wYOJdCZE130_provenance
a
np:Provenance
.
dgn-np:NP108503.RAj4cxQQ-4CtuTf_5_CBTeb-6HCZsFGa1K-L9wYOJdCZE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP108503.RAj4cxQQ-4CtuTf_5_CBTeb-6HCZsFGa1K-L9wYOJdCZE130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN95a3dc15b203730bf9ab7dfe638521de
sio:SIO_000628
miriam-gene:2147
,
lld:C0010068
;
a
sio:SIO_001122
.
}
dgn-np:NP108503.RAj4cxQQ-4CtuTf_5_CBTeb-6HCZsFGa1K-L9wYOJdCZE130_provenance
{
dgn-np:NP108503.RAj4cxQQ-4CtuTf_5_CBTeb-6HCZsFGa1K-L9wYOJdCZE130_assertion
dcterms:description
"[These findings suggest that the 20210A prothrombin allele represents an inherited risk factor for acute coronary syndrome among patients who have limited extent of coronary disease at angiography or who lack major metabolic and acquired risk factors.]. 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:11741359
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP108503.RAj4cxQQ-4CtuTf_5_CBTeb-6HCZsFGa1K-L9wYOJdCZE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:40+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" .
}