@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_assertion
a
np:Assertion
.
dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_provenance
a
np:Provenance
.
dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_assertion
{
miriam-gene:796
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNbef92a12bcede506699eac28489a12c6
sio:SIO_000628
miriam-gene:796
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_provenance
{
dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_assertion
dcterms:description
"[The aims of this study were to discover novel polymorphisms or mutations in the 5' flanking region of the human CALCA gene in Japanese subjects and to assess the association between this gene and essential hypertension (EH).]. 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:17485015
;
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 .
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dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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
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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" .
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"v2.1.0" .
}