@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM
> .
@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:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_head
{
this:
np:hasAssertion
dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_assertion
;
np:hasProvenance
dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_provenance
;
np:hasPublicationInfo
dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_assertion
a
np:Assertion
.
dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_provenance
a
np:Provenance
.
dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_assertion
{
miriam-gene:5055
a
ncit:C16612
.
lld:C0149871
a
ncit:C7057
.
dgn-gda:DGN4930a6dc9b4dd668d63253bf3ff893be
sio:SIO_000628
miriam-gene:5055
,
lld:C0149871
;
a
sio:SIO_001121
.
}
dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_provenance
{
dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_assertion
dcterms:description
"[The aim of this study was to estimate the risk of deep venous thrombosis (DVT) caused by the polymorphisms in the TAFI gene in relation to polymorphisms of the other fibrinolytic variables such as PAI-844A>G and t-PA-7,351C>T. This study includes 130 patients with DVT and 130 age- and sex-matched healthy 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:14651335
;
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:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:39+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" .
}