@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP669797.RAmgqEUEDlhXzaSiteCtiFGDlUtstlmU0nHfBlRFf9XA8
> .
@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:NP669797.RAmgqEUEDlhXzaSiteCtiFGDlUtstlmU0nHfBlRFf9XA8130_head
{
this:
np:hasAssertion
dgn-np:NP669797.RAmgqEUEDlhXzaSiteCtiFGDlUtstlmU0nHfBlRFf9XA8130_assertion
;
np:hasProvenance
dgn-np:NP669797.RAmgqEUEDlhXzaSiteCtiFGDlUtstlmU0nHfBlRFf9XA8130_provenance
;
np:hasPublicationInfo
dgn-np:NP669797.RAmgqEUEDlhXzaSiteCtiFGDlUtstlmU0nHfBlRFf9XA8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP669797.RAmgqEUEDlhXzaSiteCtiFGDlUtstlmU0nHfBlRFf9XA8130_assertion
a
np:Assertion
.
dgn-np:NP669797.RAmgqEUEDlhXzaSiteCtiFGDlUtstlmU0nHfBlRFf9XA8130_provenance
a
np:Provenance
.
dgn-np:NP669797.RAmgqEUEDlhXzaSiteCtiFGDlUtstlmU0nHfBlRFf9XA8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP669797.RAmgqEUEDlhXzaSiteCtiFGDlUtstlmU0nHfBlRFf9XA8130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN8377c6523014bb69efce7cb913a06b4a
sio:SIO_000628
miriam-gene:4846
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP669797.RAmgqEUEDlhXzaSiteCtiFGDlUtstlmU0nHfBlRFf9XA8130_provenance
{
dgn-np:NP669797.RAmgqEUEDlhXzaSiteCtiFGDlUtstlmU0nHfBlRFf9XA8130_assertion
dcterms:description
"[This SNP has previously been related to coronary heart disease, and our findings should stimulate to replication and exploration of the association of NOS3 variation with endothelial function in other settings.]. 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:18463668
;
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:NP669797.RAmgqEUEDlhXzaSiteCtiFGDlUtstlmU0nHfBlRFf9XA8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:49+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" .
}