@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP694841.RAIzUrJwcOpGrPwV2NBfHqY75PN9558jjahUCDR-C0MxM
> .
@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:NP694841.RAIzUrJwcOpGrPwV2NBfHqY75PN9558jjahUCDR-C0MxM130_head
{
this:
np:hasAssertion
dgn-np:NP694841.RAIzUrJwcOpGrPwV2NBfHqY75PN9558jjahUCDR-C0MxM130_assertion
;
np:hasProvenance
dgn-np:NP694841.RAIzUrJwcOpGrPwV2NBfHqY75PN9558jjahUCDR-C0MxM130_provenance
;
np:hasPublicationInfo
dgn-np:NP694841.RAIzUrJwcOpGrPwV2NBfHqY75PN9558jjahUCDR-C0MxM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP694841.RAIzUrJwcOpGrPwV2NBfHqY75PN9558jjahUCDR-C0MxM130_assertion
a
np:Assertion
.
dgn-np:NP694841.RAIzUrJwcOpGrPwV2NBfHqY75PN9558jjahUCDR-C0MxM130_provenance
a
np:Provenance
.
dgn-np:NP694841.RAIzUrJwcOpGrPwV2NBfHqY75PN9558jjahUCDR-C0MxM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP694841.RAIzUrJwcOpGrPwV2NBfHqY75PN9558jjahUCDR-C0MxM130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C3495426
a
ncit:C7057
.
dgn-gda:DGNfa490e40bdcf66c61c2407839e08763b
sio:SIO_000628
miriam-gene:183
,
lld:C3495426
;
a
sio:SIO_001121
.
}
dgn-np:NP694841.RAIzUrJwcOpGrPwV2NBfHqY75PN9558jjahUCDR-C0MxM130_provenance
{
dgn-np:NP694841.RAIzUrJwcOpGrPwV2NBfHqY75PN9558jjahUCDR-C0MxM130_assertion
dcterms:description
"[However, other risk factors like hyperhomocysteinemia (HCA) and single nucleotide polymorphisms involving the angiotensin converting enzyme (ACE) and angiotensinogen genes, various clotting factors etc., have yet to be established firmly as other causative factors of atherothrombotic disease.]. 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:12186157
;
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:NP694841.RAIzUrJwcOpGrPwV2NBfHqY75PN9558jjahUCDR-C0MxM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:02+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" .
}