@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP322512.RAiNo6IRNZVQfdgWVIX4cuaLHE9qRGLv1PtSZ7DwXxNBY
> .
@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:NP322512.RAiNo6IRNZVQfdgWVIX4cuaLHE9qRGLv1PtSZ7DwXxNBY130_head
{
this:
np:hasAssertion
dgn-np:NP322512.RAiNo6IRNZVQfdgWVIX4cuaLHE9qRGLv1PtSZ7DwXxNBY130_assertion
;
np:hasProvenance
dgn-np:NP322512.RAiNo6IRNZVQfdgWVIX4cuaLHE9qRGLv1PtSZ7DwXxNBY130_provenance
;
np:hasPublicationInfo
dgn-np:NP322512.RAiNo6IRNZVQfdgWVIX4cuaLHE9qRGLv1PtSZ7DwXxNBY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP322512.RAiNo6IRNZVQfdgWVIX4cuaLHE9qRGLv1PtSZ7DwXxNBY130_assertion
a
np:Assertion
.
dgn-np:NP322512.RAiNo6IRNZVQfdgWVIX4cuaLHE9qRGLv1PtSZ7DwXxNBY130_provenance
a
np:Provenance
.
dgn-np:NP322512.RAiNo6IRNZVQfdgWVIX4cuaLHE9qRGLv1PtSZ7DwXxNBY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP322512.RAiNo6IRNZVQfdgWVIX4cuaLHE9qRGLv1PtSZ7DwXxNBY130_assertion
{
miriam-gene:7447
a
ncit:C16612
.
lld:C0001430
a
ncit:C7057
.
dgn-gda:DGNdd44501d5f4ac511dff5d7a6d312efc8
sio:SIO_000628
miriam-gene:7447
,
lld:C0001430
;
a
sio:SIO_001121
.
}
dgn-np:NP322512.RAiNo6IRNZVQfdgWVIX4cuaLHE9qRGLv1PtSZ7DwXxNBY130_provenance
{
dgn-np:NP322512.RAiNo6IRNZVQfdgWVIX4cuaLHE9qRGLv1PtSZ7DwXxNBY130_assertion
dcterms:description
"[VSNL1 and CYP11B2 are 8.1- and 6.0-fold more highly expressed, respectively, in APAs harboring KCNJ5 mutations compared with those without, and the upregulation of VSNL1 in these APAs accounts for the overexpression of VSNL1 in the total APA sample set compared with normal adrenals.]. 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:22331379
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP322512.RAiNo6IRNZVQfdgWVIX4cuaLHE9qRGLv1PtSZ7DwXxNBY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:08+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" .
}