@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0
> .
@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:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_head
{
this:
np:hasAssertion
dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_assertion
;
np:hasProvenance
dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_provenance
;
np:hasPublicationInfo
dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_assertion
a
np:Assertion
.
dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_provenance
a
np:Provenance
.
dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_assertion
{
miriam-gene:5626
a
ncit:C16612
.
lld:C0001403
a
ncit:C7057
.
dgn-gda:DGNd6d8c1a7b780ce715eca9ee12d2cc4ba
sio:SIO_000628
miriam-gene:5626
,
lld:C0001403
;
a
sio:SIO_001121
.
}
dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_provenance
{
dgn-np:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_assertion
dcterms:description
"[In addition to GH, TSH, PRL and gonadotropin deficiency, patients with PROP-1 gene mutations can present with late-onset central hypocortisolism, possibly beause of the lack of important paracrine factors normally produced by the cells surrounding the corticotropes and absent in the pituitary of these patients, or because of progressive corticotrope apoptosis.]. 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:11022176
;
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:NP725090.RAg_XFPgDQjiI9A2Q3PWHCrN-pI0kZTSubcF_nCRDK3x0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}