@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP130011.RAPG6gZ5a_cTvcEE3I6zzPx21i03SWnI9_CwoLpuWvP4s
> .
@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:NP130011.RAPG6gZ5a_cTvcEE3I6zzPx21i03SWnI9_CwoLpuWvP4s130_head
{
this:
np:hasAssertion
dgn-np:NP130011.RAPG6gZ5a_cTvcEE3I6zzPx21i03SWnI9_CwoLpuWvP4s130_assertion
;
np:hasProvenance
dgn-np:NP130011.RAPG6gZ5a_cTvcEE3I6zzPx21i03SWnI9_CwoLpuWvP4s130_provenance
;
np:hasPublicationInfo
dgn-np:NP130011.RAPG6gZ5a_cTvcEE3I6zzPx21i03SWnI9_CwoLpuWvP4s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP130011.RAPG6gZ5a_cTvcEE3I6zzPx21i03SWnI9_CwoLpuWvP4s130_assertion
a
np:Assertion
.
dgn-np:NP130011.RAPG6gZ5a_cTvcEE3I6zzPx21i03SWnI9_CwoLpuWvP4s130_provenance
a
np:Provenance
.
dgn-np:NP130011.RAPG6gZ5a_cTvcEE3I6zzPx21i03SWnI9_CwoLpuWvP4s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP130011.RAPG6gZ5a_cTvcEE3I6zzPx21i03SWnI9_CwoLpuWvP4s130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGNe8e930f0f7c1836e6f5d61a2038b5fe4
sio:SIO_000628
miriam-gene:4846
,
lld:C0004153
;
a
sio:SIO_001122
.
}
dgn-np:NP130011.RAPG6gZ5a_cTvcEE3I6zzPx21i03SWnI9_CwoLpuWvP4s130_provenance
{
dgn-np:NP130011.RAPG6gZ5a_cTvcEE3I6zzPx21i03SWnI9_CwoLpuWvP4s130_assertion
dcterms:description
"[We hypothesize that the Asp allelle of the eNOS Glu298Asp polymorphism predisposes to (systemic) atherosclerosis but that the extent of the lesions, among which are those in the renal arteries, depends also on additional risk factors.]. 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:15326089
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP130011.RAPG6gZ5a_cTvcEE3I6zzPx21i03SWnI9_CwoLpuWvP4s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:07+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" .
}