@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP798476.RAyWgxT9otJIvCC47MuaGynM30uJ4v2XC3CF7C88NqPkI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP798476.RAyWgxT9otJIvCC47MuaGynM30uJ4v2XC3CF7C88NqPkI130_head
{
this:
np:hasAssertion
dgn-np:NP798476.RAyWgxT9otJIvCC47MuaGynM30uJ4v2XC3CF7C88NqPkI130_assertion
;
np:hasProvenance
dgn-np:NP798476.RAyWgxT9otJIvCC47MuaGynM30uJ4v2XC3CF7C88NqPkI130_provenance
;
np:hasPublicationInfo
dgn-np:NP798476.RAyWgxT9otJIvCC47MuaGynM30uJ4v2XC3CF7C88NqPkI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP798476.RAyWgxT9otJIvCC47MuaGynM30uJ4v2XC3CF7C88NqPkI130_assertion
a
np:Assertion
.
dgn-np:NP798476.RAyWgxT9otJIvCC47MuaGynM30uJ4v2XC3CF7C88NqPkI130_provenance
a
np:Provenance
.
dgn-np:NP798476.RAyWgxT9otJIvCC47MuaGynM30uJ4v2XC3CF7C88NqPkI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP798476.RAyWgxT9otJIvCC47MuaGynM30uJ4v2XC3CF7C88NqPkI130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0010073
a
ncit:C7057
.
dgn-gda:DGN398df208c58e8da2777d9b819926fd1b
sio:SIO_000628
miriam-gene:4846
,
lld:C0010073
;
a
sio:SIO_001122
.
}
dgn-np:NP798476.RAyWgxT9otJIvCC47MuaGynM30uJ4v2XC3CF7C88NqPkI130_provenance
{
dgn-np:NP798476.RAyWgxT9otJIvCC47MuaGynM30uJ4v2XC3CF7C88NqPkI130_assertion
dcterms:description
"[Because the endothelial nitric oxide synthase (eNOS) T-786C polymorphism is associated with reduced nitric oxide production and coronary artery spasm in Japanese patients, we speculated that it might be reversibly associated with Prinzmetal's variant angina in white Americans.]. 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:20211321
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP798476.RAyWgxT9otJIvCC47MuaGynM30uJ4v2XC3CF7C88NqPkI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:47+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}