@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49168.RA0AA7j8QmuZcSzwoJwRx9_8JxC1teB4VvMzgTKd46bJU
> .
@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:NP49168.RA0AA7j8QmuZcSzwoJwRx9_8JxC1teB4VvMzgTKd46bJU130_head
{
this:
np:hasAssertion
dgn-np:NP49168.RA0AA7j8QmuZcSzwoJwRx9_8JxC1teB4VvMzgTKd46bJU130_assertion
;
np:hasProvenance
dgn-np:NP49168.RA0AA7j8QmuZcSzwoJwRx9_8JxC1teB4VvMzgTKd46bJU130_provenance
;
np:hasPublicationInfo
dgn-np:NP49168.RA0AA7j8QmuZcSzwoJwRx9_8JxC1teB4VvMzgTKd46bJU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49168.RA0AA7j8QmuZcSzwoJwRx9_8JxC1teB4VvMzgTKd46bJU130_assertion
a
np:Assertion
.
dgn-np:NP49168.RA0AA7j8QmuZcSzwoJwRx9_8JxC1teB4VvMzgTKd46bJU130_provenance
a
np:Provenance
.
dgn-np:NP49168.RA0AA7j8QmuZcSzwoJwRx9_8JxC1teB4VvMzgTKd46bJU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49168.RA0AA7j8QmuZcSzwoJwRx9_8JxC1teB4VvMzgTKd46bJU130_assertion
{
miriam-gene:135
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNf9b9b6d7b05921ad3f2803eaa2318725
sio:SIO_000628
miriam-gene:135
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP49168.RA0AA7j8QmuZcSzwoJwRx9_8JxC1teB4VvMzgTKd46bJU130_provenance
{
dgn-np:NP49168.RA0AA7j8QmuZcSzwoJwRx9_8JxC1teB4VvMzgTKd46bJU130_assertion
dcterms:description
"[ The adenosine-related gene variants do not appear to alter susceptibility to the disease in this group of essential hypertensives. However, involvement of these genes and the adenosine system cannot be conclusively excluded from essential hypertension pathogenesis as other gene variants may still be involved.]. 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:15257174
;
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:NP49168.RA0AA7j8QmuZcSzwoJwRx9_8JxC1teB4VvMzgTKd46bJU130_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" .
}