@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP891434.RAMXq30q6lUai8G6bj5qEkgxSF42SPF0D1J-yy-t_9mto
> .
@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:NP891434.RAMXq30q6lUai8G6bj5qEkgxSF42SPF0D1J-yy-t_9mto130_head
{
this:
np:hasAssertion
dgn-np:NP891434.RAMXq30q6lUai8G6bj5qEkgxSF42SPF0D1J-yy-t_9mto130_assertion
;
np:hasProvenance
dgn-np:NP891434.RAMXq30q6lUai8G6bj5qEkgxSF42SPF0D1J-yy-t_9mto130_provenance
;
np:hasPublicationInfo
dgn-np:NP891434.RAMXq30q6lUai8G6bj5qEkgxSF42SPF0D1J-yy-t_9mto130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP891434.RAMXq30q6lUai8G6bj5qEkgxSF42SPF0D1J-yy-t_9mto130_assertion
a
np:Assertion
.
dgn-np:NP891434.RAMXq30q6lUai8G6bj5qEkgxSF42SPF0D1J-yy-t_9mto130_provenance
a
np:Provenance
.
dgn-np:NP891434.RAMXq30q6lUai8G6bj5qEkgxSF42SPF0D1J-yy-t_9mto130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP891434.RAMXq30q6lUai8G6bj5qEkgxSF42SPF0D1J-yy-t_9mto130_assertion
{
miriam-gene:1585
a
ncit:C16612
.
lld:C0015544
a
ncit:C7057
.
dgn-gda:DGNc97f91be1740ac81f88f236fbc947d46
sio:SIO_000628
miriam-gene:1585
,
lld:C0015544
;
a
sio:SIO_001121
.
}
dgn-np:NP891434.RAMXq30q6lUai8G6bj5qEkgxSF42SPF0D1J-yy-t_9mto130_provenance
{
dgn-np:NP891434.RAMXq30q6lUai8G6bj5qEkgxSF42SPF0D1J-yy-t_9mto130_assertion
dcterms:description
"[Mutations in CYP11B2 result in aldosterone synthase (corticosterone methyloxidase) deficiency, an isolated defect in aldosterone biosynthesis that can cause hyponatremia, hyperkalemia, and hypovolemic shock in infancy and failure to thrive in childhood.]. 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:7988480
;
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:NP891434.RAMXq30q6lUai8G6bj5qEkgxSF42SPF0D1J-yy-t_9mto130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:08+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" .
}