@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ
> .
@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:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_head
{
this:
np:hasAssertion
dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_assertion
;
np:hasProvenance
dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_assertion
a
np:Assertion
.
dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_provenance
a
np:Provenance
.
dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0010072
a
ncit:C7057
.
dgn-gda:DGNd23c0279ff5a9b41e575ac008addd8d3
sio:SIO_000628
miriam-gene:183
,
lld:C0010072
;
a
sio:SIO_001122
.
}
dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_provenance
{
dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_assertion
dcterms:description
"[To investigate the distribution frequencies of angiotensin-converting enzyme (ACE), angiotensinogen (AGT), angiotensin II I type receptor (AT1R) genotypes in Chinese, to find the relationships between polymorphisms of ACE, AGT and AT1R gene, and coronary artery thrombosis disease (CATD) and to study the interactions of themselves, PCR and PCR-RFLP techniques were performed to determine the genotypes of ACE, AGT and AT1R gene in CATD group (192 cases) and control group (110 cases).]. 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:15498133
;
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:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_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" .
}