@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME
> .
@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:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_head
{
this:
np:hasAssertion
dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_assertion
;
np:hasProvenance
dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_provenance
;
np:hasPublicationInfo
dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_assertion
a
np:Assertion
.
dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_provenance
a
np:Provenance
.
dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_assertion
{
miriam-gene:4072
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN3676b18c57de51f8c32762b3b0ccdc18
sio:SIO_000628
miriam-gene:4072
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_provenance
{
dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_assertion
dcterms:description
"[Further larger studies are needed to (1) estimate the prevalence of this mutant among individuals belonging to different KSA locations (2) assess the relative contribution of this mutational event separately and in combination with other thrombophilic polymorphisms in the etiology of cardiovascular disease in KSA.]. 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:21553052
;
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 .
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dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:31+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" .
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pav:version
"v2.1.0" .
}