@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg
> .
@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:NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_head
{
this:
np:hasAssertion
dgn-np:NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_assertion
;
np:hasProvenance
dgn-np:NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_provenance
;
np:hasPublicationInfo
dgn-np:NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_assertion
a
np:Assertion
.
dgn-np:NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_provenance
a
np:Provenance
.
dgn-np:NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN82462d7846617ce665d2e295868d7a01
sio:SIO_000628
miriam-gene:183
,
lld:C1956346
;
a
sio:SIO_001122
.
}
dgn-np:NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_provenance
{
dgn-np:NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_assertion
dcterms:description
"[To investigate the role of haplotypes formed by these polymorphisms for angiotensinogen levels we examined blood pressure, coronary artery disease (CAD), myocardial infarction (MI), and AGT genotypes and haplotypes in 2,575 patients with angiographically documented CAD and 731 individuals in whom CAD had been ruled out by angiography.]. 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:15599691
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48893.RAdrhBdEN3Pl9jp_NAwKleCyN-S8-x8-IIQQIldF7z2Eg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}