@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g
> .
@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:NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_head
{
this:
np:hasAssertion
dgn-np:NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_assertion
;
np:hasProvenance
dgn-np:NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_provenance
;
np:hasPublicationInfo
dgn-np:NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_assertion
a
np:Assertion
.
dgn-np:NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_provenance
a
np:Provenance
.
dgn-np:NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_assertion
{
miriam-gene:119
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN5974f1fff20293d70921085e8d175199
sio:SIO_000628
miriam-gene:119
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_provenance
{
dgn-np:NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_assertion
dcterms:description
"[Our findings suggest that hypertension candidate gene variation may influence BP responses to specific antihypertensive drug therapies and measurement of genetic variation may assist in identifying subgroups of hypertensive patients who will benefit most from particular antihypertensive drug therapies.]. 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:17854487
;
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:NP49278.RAWwPNTWLhscE2W0k-a5TZctvitPV78bmyI4IJLX0vG2g130_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" .
}