@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP275308.RAUgqPprq7HBvMFY6Ea0bD4OE7fwUGpRjkvZaS3VT3yyg
> .
@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:NP275308.RAUgqPprq7HBvMFY6Ea0bD4OE7fwUGpRjkvZaS3VT3yyg130_head
{
this:
np:hasAssertion
dgn-np:NP275308.RAUgqPprq7HBvMFY6Ea0bD4OE7fwUGpRjkvZaS3VT3yyg130_assertion
;
np:hasProvenance
dgn-np:NP275308.RAUgqPprq7HBvMFY6Ea0bD4OE7fwUGpRjkvZaS3VT3yyg130_provenance
;
np:hasPublicationInfo
dgn-np:NP275308.RAUgqPprq7HBvMFY6Ea0bD4OE7fwUGpRjkvZaS3VT3yyg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP275308.RAUgqPprq7HBvMFY6Ea0bD4OE7fwUGpRjkvZaS3VT3yyg130_assertion
a
np:Assertion
.
dgn-np:NP275308.RAUgqPprq7HBvMFY6Ea0bD4OE7fwUGpRjkvZaS3VT3yyg130_provenance
a
np:Provenance
.
dgn-np:NP275308.RAUgqPprq7HBvMFY6Ea0bD4OE7fwUGpRjkvZaS3VT3yyg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP275308.RAUgqPprq7HBvMFY6Ea0bD4OE7fwUGpRjkvZaS3VT3yyg130_assertion
{
miriam-gene:959
a
ncit:C16612
.
lld:C0042974
a
ncit:C7057
.
dgn-gda:DGN58b491494d47a385525516ce63d2bd5b
sio:SIO_000628
miriam-gene:959
,
lld:C0042974
;
a
sio:SIO_001121
.
}
dgn-np:NP275308.RAUgqPprq7HBvMFY6Ea0bD4OE7fwUGpRjkvZaS3VT3yyg130_provenance
{
dgn-np:NP275308.RAUgqPprq7HBvMFY6Ea0bD4OE7fwUGpRjkvZaS3VT3yyg130_assertion
dcterms:description
"[807T allele is an independent predictor for sCD40L levels during the acute phase of premature MI as well as one year after the event, while it is associated with elevated sCD40L levels in healthy subjects, only in the presence of high von Willebrand levels.]. 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:16697311
;
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:NP275308.RAUgqPprq7HBvMFY6Ea0bD4OE7fwUGpRjkvZaS3VT3yyg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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" .
}