@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP24361.RA0xWtImX-FO_EykgK6VeGWsFiOQmiFl15enONbuQxEqI
> .
@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:NP24361.RA0xWtImX-FO_EykgK6VeGWsFiOQmiFl15enONbuQxEqI130_head
{
this:
np:hasAssertion
dgn-np:NP24361.RA0xWtImX-FO_EykgK6VeGWsFiOQmiFl15enONbuQxEqI130_assertion
;
np:hasProvenance
dgn-np:NP24361.RA0xWtImX-FO_EykgK6VeGWsFiOQmiFl15enONbuQxEqI130_provenance
;
np:hasPublicationInfo
dgn-np:NP24361.RA0xWtImX-FO_EykgK6VeGWsFiOQmiFl15enONbuQxEqI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP24361.RA0xWtImX-FO_EykgK6VeGWsFiOQmiFl15enONbuQxEqI130_assertion
a
np:Assertion
.
dgn-np:NP24361.RA0xWtImX-FO_EykgK6VeGWsFiOQmiFl15enONbuQxEqI130_provenance
a
np:Provenance
.
dgn-np:NP24361.RA0xWtImX-FO_EykgK6VeGWsFiOQmiFl15enONbuQxEqI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP24361.RA0xWtImX-FO_EykgK6VeGWsFiOQmiFl15enONbuQxEqI130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0010073
a
ncit:C7057
.
dgn-gda:DGN7a0c568f1c6c74716b90b23684f0a35d
sio:SIO_000628
miriam-gene:4846
,
lld:C0010073
;
a
sio:SIO_001121
.
}
dgn-np:NP24361.RA0xWtImX-FO_EykgK6VeGWsFiOQmiFl15enONbuQxEqI130_provenance
{
dgn-np:NP24361.RA0xWtImX-FO_EykgK6VeGWsFiOQmiFl15enONbuQxEqI130_assertion
dcterms:description
"[The purpose of this study has been to elucidate the possible variants that occur in the coding region of the endothelial nitric oxide synthase (eNOS) gene and that may be associated with coronary spasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:9737779
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP24361.RA0xWtImX-FO_EykgK6VeGWsFiOQmiFl15enONbuQxEqI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:09+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" .
}