@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw
> .
@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:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_head
{
this:
np:hasAssertion
dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_assertion
;
np:hasProvenance
dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_provenance
;
np:hasPublicationInfo
dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_assertion
a
np:Assertion
.
dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_provenance
a
np:Provenance
.
dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN0ff79f660b21596f78943a0c8c0a3e52
sio:SIO_000628
miriam-gene:4846
,
lld:C0007222
;
a
sio:SIO_001122
.
}
dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_provenance
{
dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_assertion
dcterms:description
"[Thus, in the Moscow population the ecNOS4a/4b VNTR of the NOS3 gene and the A1166C polymorphism of the AT1 gene are associated with the IHD development. Furthermore, the correlation with the IHD revealed was much stronger for the NOS3 VNTR locus.]. 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:11190479
;
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:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}