@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP724853.RAn7s9cy3XLKFFOJ2GbMR-9ikmTv2Q9jsZ5Z56cXCIAnY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP724853.RAn7s9cy3XLKFFOJ2GbMR-9ikmTv2Q9jsZ5Z56cXCIAnY130_head
{
this:
np:hasAssertion
dgn-np:NP724853.RAn7s9cy3XLKFFOJ2GbMR-9ikmTv2Q9jsZ5Z56cXCIAnY130_assertion
;
np:hasProvenance
dgn-np:NP724853.RAn7s9cy3XLKFFOJ2GbMR-9ikmTv2Q9jsZ5Z56cXCIAnY130_provenance
;
np:hasPublicationInfo
dgn-np:NP724853.RAn7s9cy3XLKFFOJ2GbMR-9ikmTv2Q9jsZ5Z56cXCIAnY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP724853.RAn7s9cy3XLKFFOJ2GbMR-9ikmTv2Q9jsZ5Z56cXCIAnY130_assertion
a
np:Assertion
.
dgn-np:NP724853.RAn7s9cy3XLKFFOJ2GbMR-9ikmTv2Q9jsZ5Z56cXCIAnY130_provenance
a
np:Provenance
.
dgn-np:NP724853.RAn7s9cy3XLKFFOJ2GbMR-9ikmTv2Q9jsZ5Z56cXCIAnY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP724853.RAn7s9cy3XLKFFOJ2GbMR-9ikmTv2Q9jsZ5Z56cXCIAnY130_assertion
{
miriam-gene:6927
a
ncit:C16612
.
lld:C0311277
a
ncit:C7057
.
dgn-gda:DGN358f68fc965468b7f92827d3e1fe1e25
sio:SIO_000628
miriam-gene:6927
,
lld:C0311277
;
a
sio:SIO_001122
.
}
dgn-np:NP724853.RAn7s9cy3XLKFFOJ2GbMR-9ikmTv2Q9jsZ5Z56cXCIAnY130_provenance
{
dgn-np:NP724853.RAn7s9cy3XLKFFOJ2GbMR-9ikmTv2Q9jsZ5Z56cXCIAnY130_assertion
dcterms:description
"[Analysis of statistically similar SNPs suggested that the causative variants for systolic blood pressure were located in F11R, whilst those for central obesity could be due to causative variants in the transcription factor 1 gene immediately upstream.]. 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:18067551
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP724853.RAn7s9cy3XLKFFOJ2GbMR-9ikmTv2Q9jsZ5Z56cXCIAnY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:57+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}