@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48673.RA3h7U1zhHb1Xpg-iWEQ1DU-xlDQ3dTSLRVBPK02DG_pg
> .
@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:NP48673.RA3h7U1zhHb1Xpg-iWEQ1DU-xlDQ3dTSLRVBPK02DG_pg130_head
{
this:
np:hasAssertion
dgn-np:NP48673.RA3h7U1zhHb1Xpg-iWEQ1DU-xlDQ3dTSLRVBPK02DG_pg130_assertion
;
np:hasProvenance
dgn-np:NP48673.RA3h7U1zhHb1Xpg-iWEQ1DU-xlDQ3dTSLRVBPK02DG_pg130_provenance
;
np:hasPublicationInfo
dgn-np:NP48673.RA3h7U1zhHb1Xpg-iWEQ1DU-xlDQ3dTSLRVBPK02DG_pg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48673.RA3h7U1zhHb1Xpg-iWEQ1DU-xlDQ3dTSLRVBPK02DG_pg130_assertion
a
np:Assertion
.
dgn-np:NP48673.RA3h7U1zhHb1Xpg-iWEQ1DU-xlDQ3dTSLRVBPK02DG_pg130_provenance
a
np:Provenance
.
dgn-np:NP48673.RA3h7U1zhHb1Xpg-iWEQ1DU-xlDQ3dTSLRVBPK02DG_pg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48673.RA3h7U1zhHb1Xpg-iWEQ1DU-xlDQ3dTSLRVBPK02DG_pg130_assertion
{
miriam-gene:217
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN98287d23ce3db1540bb19fbc11ee8f04
sio:SIO_000628
miriam-gene:217
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP48673.RA3h7U1zhHb1Xpg-iWEQ1DU-xlDQ3dTSLRVBPK02DG_pg130_provenance
{
dgn-np:NP48673.RA3h7U1zhHb1Xpg-iWEQ1DU-xlDQ3dTSLRVBPK02DG_pg130_assertion
dcterms:description
"[These results suggest that the Glu/Glu genotype is a potent risk factor for hypertension among males mainly through its association with the level of alcohol consumption, and that the ALDH2 genotype does not affect the sensitivity to the pressor effects of alcohol.]. 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:11510748
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48673.RA3h7U1zhHb1Xpg-iWEQ1DU-xlDQ3dTSLRVBPK02DG_pg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}