@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY
> .
@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:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_head
{
this:
np:hasAssertion
dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_assertion
;
np:hasProvenance
dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_provenance
;
np:hasPublicationInfo
dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_assertion
a
np:Assertion
.
dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_provenance
a
np:Provenance
.
dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN4c8db4029ffd006784aeaa1710f5c6b3
sio:SIO_000628
miriam-gene:4846
,
lld:C0027051
;
a
sio:SIO_001122
.
}
dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_provenance
{
dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_assertion
dcterms:description
"[This study indicates that E298D polymorphism of the eNOS gene seems to be associated with MI occurrence in the Greek population. It is possible that TT genotype is closely linked to the etiology of MI even after adjusting for known MI risk factors.]. 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:20854685
;
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:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_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" .
}