@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP936844.RAEmGyVlnbqTCiyRq-KZaCVjnMKsiwIOf3l7AZSXot0os
> .
@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 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:NP936844.RAEmGyVlnbqTCiyRq-KZaCVjnMKsiwIOf3l7AZSXot0os130_head
{
this:
np:hasAssertion
dgn-np:NP936844.RAEmGyVlnbqTCiyRq-KZaCVjnMKsiwIOf3l7AZSXot0os130_assertion
;
np:hasProvenance
dgn-np:NP936844.RAEmGyVlnbqTCiyRq-KZaCVjnMKsiwIOf3l7AZSXot0os130_provenance
;
np:hasPublicationInfo
dgn-np:NP936844.RAEmGyVlnbqTCiyRq-KZaCVjnMKsiwIOf3l7AZSXot0os130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP936844.RAEmGyVlnbqTCiyRq-KZaCVjnMKsiwIOf3l7AZSXot0os130_assertion
a
np:Assertion
.
dgn-np:NP936844.RAEmGyVlnbqTCiyRq-KZaCVjnMKsiwIOf3l7AZSXot0os130_provenance
a
np:Provenance
.
dgn-np:NP936844.RAEmGyVlnbqTCiyRq-KZaCVjnMKsiwIOf3l7AZSXot0os130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP936844.RAEmGyVlnbqTCiyRq-KZaCVjnMKsiwIOf3l7AZSXot0os130_assertion
{
miriam-gene:3769
a
ncit:C16612
.
lld:C3272363
a
ncit:C7057
.
dgn-gda:DGNdc80efa1f1f199f965ee52a7d98a2b46
sio:SIO_000628
miriam-gene:3769
,
lld:C3272363
;
a
sio:SIO_001121
.
}
dgn-np:NP936844.RAEmGyVlnbqTCiyRq-KZaCVjnMKsiwIOf3l7AZSXot0os130_provenance
{
dgn-np:NP936844.RAEmGyVlnbqTCiyRq-KZaCVjnMKsiwIOf3l7AZSXot0os130_assertion
dct:description
"[The aim of the study was to investigate the association between the FXIII Val34Leu polymorphism and the risk of ischemic stroke due to small vessel disease (SVD) or the risk of primary intracerebral hemorrhage (PICH).]. 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:15644629
;
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:NP936844.RAEmGyVlnbqTCiyRq-KZaCVjnMKsiwIOf3l7AZSXot0os130_publicationInfo
{
this:
dct:created
"2014-10-02T12:41:34+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct: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" .
}