@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP602726.RAn7E9FMSP6DWUdc3H8Uwh6C7DN0_KGfzTPyQ8w_OQ7AA
> .
@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:NP602726.RAn7E9FMSP6DWUdc3H8Uwh6C7DN0_KGfzTPyQ8w_OQ7AA130_head
{
this:
np:hasAssertion
dgn-np:NP602726.RAn7E9FMSP6DWUdc3H8Uwh6C7DN0_KGfzTPyQ8w_OQ7AA130_assertion
;
np:hasProvenance
dgn-np:NP602726.RAn7E9FMSP6DWUdc3H8Uwh6C7DN0_KGfzTPyQ8w_OQ7AA130_provenance
;
np:hasPublicationInfo
dgn-np:NP602726.RAn7E9FMSP6DWUdc3H8Uwh6C7DN0_KGfzTPyQ8w_OQ7AA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP602726.RAn7E9FMSP6DWUdc3H8Uwh6C7DN0_KGfzTPyQ8w_OQ7AA130_assertion
a
np:Assertion
.
dgn-np:NP602726.RAn7E9FMSP6DWUdc3H8Uwh6C7DN0_KGfzTPyQ8w_OQ7AA130_provenance
a
np:Provenance
.
dgn-np:NP602726.RAn7E9FMSP6DWUdc3H8Uwh6C7DN0_KGfzTPyQ8w_OQ7AA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP602726.RAn7E9FMSP6DWUdc3H8Uwh6C7DN0_KGfzTPyQ8w_OQ7AA130_assertion
{
miriam-gene:342977
a
ncit:C16612
.
lld:C0598608
a
ncit:C7057
.
dgn-gda:DGNbbfe32dee47bc7a72ac852e5a1fe09ac
sio:SIO_000628
miriam-gene:342977
,
lld:C0598608
;
a
sio:SIO_001121
.
}
dgn-np:NP602726.RAn7E9FMSP6DWUdc3H8Uwh6C7DN0_KGfzTPyQ8w_OQ7AA130_provenance
{
dgn-np:NP602726.RAn7E9FMSP6DWUdc3H8Uwh6C7DN0_KGfzTPyQ8w_OQ7AA130_assertion
dcterms:description
"[Nitric oxide (NO) plays a relevant role in various events during atherogenesis, and in vitro data suggest that NO may modulate total homocysteine (tHcy) concentrations, whereas polymorphisms of the endothelial nitric oxide (NOS3) gene have been reported to be related to an increased risk of myocardial infarction (MI) and hyperhomocysteinemia, but the results have been controversial.]. 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:22652373
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP602726.RAn7E9FMSP6DWUdc3H8Uwh6C7DN0_KGfzTPyQ8w_OQ7AA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:02+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" .
}