@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP324794.RAmSYz-EYeJrJuddyFsP__qkS9QAdN6r8J4uIOqgmcwDc
> .
@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:NP324794.RAmSYz-EYeJrJuddyFsP__qkS9QAdN6r8J4uIOqgmcwDc130_head
{
this:
np:hasAssertion
dgn-np:NP324794.RAmSYz-EYeJrJuddyFsP__qkS9QAdN6r8J4uIOqgmcwDc130_assertion
;
np:hasProvenance
dgn-np:NP324794.RAmSYz-EYeJrJuddyFsP__qkS9QAdN6r8J4uIOqgmcwDc130_provenance
;
np:hasPublicationInfo
dgn-np:NP324794.RAmSYz-EYeJrJuddyFsP__qkS9QAdN6r8J4uIOqgmcwDc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP324794.RAmSYz-EYeJrJuddyFsP__qkS9QAdN6r8J4uIOqgmcwDc130_assertion
a
np:Assertion
.
dgn-np:NP324794.RAmSYz-EYeJrJuddyFsP__qkS9QAdN6r8J4uIOqgmcwDc130_provenance
a
np:Provenance
.
dgn-np:NP324794.RAmSYz-EYeJrJuddyFsP__qkS9QAdN6r8J4uIOqgmcwDc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP324794.RAmSYz-EYeJrJuddyFsP__qkS9QAdN6r8J4uIOqgmcwDc130_assertion
{
miriam-gene:7450
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN12ac425d5914c4f0bc909679ec6a3e11
sio:SIO_000628
miriam-gene:7450
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP324794.RAmSYz-EYeJrJuddyFsP__qkS9QAdN6r8J4uIOqgmcwDc130_provenance
{
dgn-np:NP324794.RAmSYz-EYeJrJuddyFsP__qkS9QAdN6r8J4uIOqgmcwDc130_assertion
dcterms:description
"[However, as studies frequently differ in design, population and endpoint, and are often underpowered, it remains unclear whether VWF is causally related to the occurrence of arterial thrombosis or primarily mirrors endothelial dysfunction, which predisposes to atherosclerosis and subsequent arterial thrombosis.]. 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:21342431
;
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:NP324794.RAmSYz-EYeJrJuddyFsP__qkS9QAdN6r8J4uIOqgmcwDc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:10+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" .
}