@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP932323.RAHzpVdqTfkuUpgKGaRqNxQ4rYVptCH8Uhv32ocNasuwI
> .
@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:NP932323.RAHzpVdqTfkuUpgKGaRqNxQ4rYVptCH8Uhv32ocNasuwI130_head
{
this:
np:hasAssertion
dgn-np:NP932323.RAHzpVdqTfkuUpgKGaRqNxQ4rYVptCH8Uhv32ocNasuwI130_assertion
;
np:hasProvenance
dgn-np:NP932323.RAHzpVdqTfkuUpgKGaRqNxQ4rYVptCH8Uhv32ocNasuwI130_provenance
;
np:hasPublicationInfo
dgn-np:NP932323.RAHzpVdqTfkuUpgKGaRqNxQ4rYVptCH8Uhv32ocNasuwI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP932323.RAHzpVdqTfkuUpgKGaRqNxQ4rYVptCH8Uhv32ocNasuwI130_assertion
a
np:Assertion
.
dgn-np:NP932323.RAHzpVdqTfkuUpgKGaRqNxQ4rYVptCH8Uhv32ocNasuwI130_provenance
a
np:Provenance
.
dgn-np:NP932323.RAHzpVdqTfkuUpgKGaRqNxQ4rYVptCH8Uhv32ocNasuwI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP932323.RAHzpVdqTfkuUpgKGaRqNxQ4rYVptCH8Uhv32ocNasuwI130_assertion
{
miriam-gene:5443
a
ncit:C16612
.
lld:C0034013
a
ncit:C7057
.
dgn-gda:DGNda906af50ea1883c7e856ea281c481a7
sio:SIO_000628
miriam-gene:5443
,
lld:C0034013
;
a
sio:SIO_001121
.
}
dgn-np:NP932323.RAHzpVdqTfkuUpgKGaRqNxQ4rYVptCH8Uhv32ocNasuwI130_provenance
{
dgn-np:NP932323.RAHzpVdqTfkuUpgKGaRqNxQ4rYVptCH8Uhv32ocNasuwI130_assertion
dcterms:description
"[In conclusion, peripheral precocious puberty in patients with DAX1 gene mutations appears to be secondary to the stimulus exerted by ACTH on melanocortin receptors in Leydig cells and to the overexpression of testicular steroidogenesis activators by the loss of transcriptional repression.]. 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:18414894
;
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:NP932323.RAHzpVdqTfkuUpgKGaRqNxQ4rYVptCH8Uhv32ocNasuwI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:31+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" .
}