@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP846747.RAgr9HAAwYcn9pa1N2WznVcnZa6Rc76E89lCCjMvrLSZs
> .
@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:NP846747.RAgr9HAAwYcn9pa1N2WznVcnZa6Rc76E89lCCjMvrLSZs130_head
{
this:
np:hasAssertion
dgn-np:NP846747.RAgr9HAAwYcn9pa1N2WznVcnZa6Rc76E89lCCjMvrLSZs130_assertion
;
np:hasProvenance
dgn-np:NP846747.RAgr9HAAwYcn9pa1N2WznVcnZa6Rc76E89lCCjMvrLSZs130_provenance
;
np:hasPublicationInfo
dgn-np:NP846747.RAgr9HAAwYcn9pa1N2WznVcnZa6Rc76E89lCCjMvrLSZs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP846747.RAgr9HAAwYcn9pa1N2WznVcnZa6Rc76E89lCCjMvrLSZs130_assertion
a
np:Assertion
.
dgn-np:NP846747.RAgr9HAAwYcn9pa1N2WznVcnZa6Rc76E89lCCjMvrLSZs130_provenance
a
np:Provenance
.
dgn-np:NP846747.RAgr9HAAwYcn9pa1N2WznVcnZa6Rc76E89lCCjMvrLSZs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP846747.RAgr9HAAwYcn9pa1N2WznVcnZa6Rc76E89lCCjMvrLSZs130_assertion
{
miriam-gene:4158
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN2762e406b729a9d0a368d5a339b2000a
sio:SIO_000628
miriam-gene:4158
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP846747.RAgr9HAAwYcn9pa1N2WznVcnZa6Rc76E89lCCjMvrLSZs130_provenance
{
dgn-np:NP846747.RAgr9HAAwYcn9pa1N2WznVcnZa6Rc76E89lCCjMvrLSZs130_assertion
dcterms:description
"[Familial Glucocorticoid deficiency (FGD), in which the adrenal cortex fails to produce glucocorticoids, was first shown to be caused by defects in the receptor for ACTH (MC2R) or its accessory protein (MRAP).]. 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:23279877
;
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:NP846747.RAgr9HAAwYcn9pa1N2WznVcnZa6Rc76E89lCCjMvrLSZs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:37+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" .
}