@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48845.RAVUXl1kB80gFTVumcTuCMPZdh4zRGW5xxoQe-LXYbANg
> .
@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:NP48845.RAVUXl1kB80gFTVumcTuCMPZdh4zRGW5xxoQe-LXYbANg130_head
{
this:
np:hasAssertion
dgn-np:NP48845.RAVUXl1kB80gFTVumcTuCMPZdh4zRGW5xxoQe-LXYbANg130_assertion
;
np:hasProvenance
dgn-np:NP48845.RAVUXl1kB80gFTVumcTuCMPZdh4zRGW5xxoQe-LXYbANg130_provenance
;
np:hasPublicationInfo
dgn-np:NP48845.RAVUXl1kB80gFTVumcTuCMPZdh4zRGW5xxoQe-LXYbANg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48845.RAVUXl1kB80gFTVumcTuCMPZdh4zRGW5xxoQe-LXYbANg130_assertion
a
np:Assertion
.
dgn-np:NP48845.RAVUXl1kB80gFTVumcTuCMPZdh4zRGW5xxoQe-LXYbANg130_provenance
a
np:Provenance
.
dgn-np:NP48845.RAVUXl1kB80gFTVumcTuCMPZdh4zRGW5xxoQe-LXYbANg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48845.RAVUXl1kB80gFTVumcTuCMPZdh4zRGW5xxoQe-LXYbANg130_assertion
{
miriam-gene:185
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN847171a5d656e9384392cd9c4a7a3da1
sio:SIO_000628
miriam-gene:185
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP48845.RAVUXl1kB80gFTVumcTuCMPZdh4zRGW5xxoQe-LXYbANg130_provenance
{
dgn-np:NP48845.RAVUXl1kB80gFTVumcTuCMPZdh4zRGW5xxoQe-LXYbANg130_assertion
dcterms:description
"[ These results suggest that the AGT and AT1 receptor genes are not major genetic determinants of hypertension associated with NIDDM in this population, although we can not exclude the possibility that these loci make a minor contribution in a polygenic context.]. 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:9218178
;
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:NP48845.RAVUXl1kB80gFTVumcTuCMPZdh4zRGW5xxoQe-LXYbANg130_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" .
}