@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ
> .
@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:NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_head
{
this:
np:hasAssertion
dgn-np:NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_assertion
;
np:hasProvenance
dgn-np:NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_assertion
a
np:Assertion
.
dgn-np:NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_provenance
a
np:Provenance
.
dgn-np:NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_assertion
{
miriam-gene:4158
a
ncit:C16612
.
lld:C1955741
a
ncit:C7057
.
dgn-gda:DGNc6e32c6d416468d28de7185dc0001f05
sio:SIO_000628
miriam-gene:4158
,
lld:C1955741
;
a
sio:SIO_001121
.
}
dgn-np:NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_provenance
{
dgn-np:NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_assertion
dcterms:description
"[This would be similar to the clinical findings in familial glucocorticoid deficiency type 1, an autosomal recessive condition due to inactivating mutations of the adrenal receptor for ACTH, also known as the melanocortin 2 receptor (MC2R).]. 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:19931309
;
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:NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:04+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" .
}