@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP932493.RA6_LkQVLk1Kd5TKlszxGVS7DdOeeFocta9dExgiNXBx8
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP932493.RA6_LkQVLk1Kd5TKlszxGVS7DdOeeFocta9dExgiNXBx8130_assertion
;
np:hasProvenance
dgn-np:NP932493.RA6_LkQVLk1Kd5TKlszxGVS7DdOeeFocta9dExgiNXBx8130_provenance
;
np:hasPublicationInfo
dgn-np:NP932493.RA6_LkQVLk1Kd5TKlszxGVS7DdOeeFocta9dExgiNXBx8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP932493.RA6_LkQVLk1Kd5TKlszxGVS7DdOeeFocta9dExgiNXBx8130_assertion
a
np:Assertion
.
dgn-np:NP932493.RA6_LkQVLk1Kd5TKlszxGVS7DdOeeFocta9dExgiNXBx8130_provenance
a
np:Provenance
.
dgn-np:NP932493.RA6_LkQVLk1Kd5TKlszxGVS7DdOeeFocta9dExgiNXBx8130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:4846
a
ncit:C16612
.
lld:C2733225
a
ncit:C7057
.
dgn-gda:DGN106427ea1630afe44ff3707832d25133
sio:SIO_000628
miriam-gene:4846
,
lld:C2733225
;
a
sio:SIO_001121
.
}
dgn-np:NP932493.RA6_LkQVLk1Kd5TKlszxGVS7DdOeeFocta9dExgiNXBx8130_provenance
{
dgn-np:NP932493.RA6_LkQVLk1Kd5TKlszxGVS7DdOeeFocta9dExgiNXBx8130_assertion
dcterms:description
"[Since reduced NO synthesis in endothelial cells has been implicated in the development of coronary atherosclerosis, we investigated the association of NOS3 gene polymorphisms and coronary artery disease (CAD) in an Iranian population.]. 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:20103956
;
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:NP932493.RA6_LkQVLk1Kd5TKlszxGVS7DdOeeFocta9dExgiNXBx8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:31+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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"v2.1.0" .
}