@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP214699.RAw3I7_h7PhrMgLiEO9Kw_UXAfumSGaQ_DOopRVZ2hAyU
> .
@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:NP214699.RAw3I7_h7PhrMgLiEO9Kw_UXAfumSGaQ_DOopRVZ2hAyU130_head
{
this:
np:hasAssertion
dgn-np:NP214699.RAw3I7_h7PhrMgLiEO9Kw_UXAfumSGaQ_DOopRVZ2hAyU130_assertion
;
np:hasProvenance
dgn-np:NP214699.RAw3I7_h7PhrMgLiEO9Kw_UXAfumSGaQ_DOopRVZ2hAyU130_provenance
;
np:hasPublicationInfo
dgn-np:NP214699.RAw3I7_h7PhrMgLiEO9Kw_UXAfumSGaQ_DOopRVZ2hAyU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP214699.RAw3I7_h7PhrMgLiEO9Kw_UXAfumSGaQ_DOopRVZ2hAyU130_assertion
a
np:Assertion
.
dgn-np:NP214699.RAw3I7_h7PhrMgLiEO9Kw_UXAfumSGaQ_DOopRVZ2hAyU130_provenance
a
np:Provenance
.
dgn-np:NP214699.RAw3I7_h7PhrMgLiEO9Kw_UXAfumSGaQ_DOopRVZ2hAyU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP214699.RAw3I7_h7PhrMgLiEO9Kw_UXAfumSGaQ_DOopRVZ2hAyU130_assertion
{
miriam-gene:1584
a
ncit:C16612
.
lld:C0020428
a
ncit:C7057
.
dgn-gda:DGN591b2e98aadf4a05dbb2f406c20388e0
sio:SIO_000628
miriam-gene:1584
,
lld:C0020428
;
a
sio:SIO_001121
.
}
dgn-np:NP214699.RAw3I7_h7PhrMgLiEO9Kw_UXAfumSGaQ_DOopRVZ2hAyU130_provenance
{
dgn-np:NP214699.RAw3I7_h7PhrMgLiEO9Kw_UXAfumSGaQ_DOopRVZ2hAyU130_assertion
dcterms:description
"[Although a chimeric gene combining the 11beta-hydroxylase gene (CYP11B1) and the aldosterone synthase gene (CYP11B2) explains the pathophysiology of familial hyperaldosteronism (FH) type I, the contribution of this abnormality to FH type II has not been tested.]. 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:11453962
;
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:NP214699.RAw3I7_h7PhrMgLiEO9Kw_UXAfumSGaQ_DOopRVZ2hAyU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:59+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" .
}