@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio
> .
@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:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_head
{
this:
np:hasAssertion
dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_assertion
;
np:hasProvenance
dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_provenance
;
np:hasPublicationInfo
dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_assertion
a
np:Assertion
.
dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_provenance
a
np:Provenance
.
dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0010073
a
ncit:C7057
.
dgn-gda:DGNa04351ad4779dadf508ca5ba7e1eb386
sio:SIO_000628
miriam-gene:4846
,
lld:C0010073
;
a
sio:SIO_001121
.
}
dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_provenance
{
dgn-np:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_assertion
dcterms:description
"[Multiple logistic regression analysis with forward stepwise selection using the environmental risk factors and the eNOS gene variant revealed that the most predictive independent risk factor for coronary spasm was the mutant allele (P<0.0001).]. 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:10359729
;
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:NP24360.RAiQZygmgYS8JH8TZ1MV7lgwAvYcmZPJCcVDBtajPLhio130_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" .
}