@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP686047.RASjz8lHwwcnYMkf8Rg4Ighxj3MwdWnfZ07PrOYjhKEa4
> .
@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:NP686047.RASjz8lHwwcnYMkf8Rg4Ighxj3MwdWnfZ07PrOYjhKEa4130_head
{
this:
np:hasAssertion
dgn-np:NP686047.RASjz8lHwwcnYMkf8Rg4Ighxj3MwdWnfZ07PrOYjhKEa4130_assertion
;
np:hasProvenance
dgn-np:NP686047.RASjz8lHwwcnYMkf8Rg4Ighxj3MwdWnfZ07PrOYjhKEa4130_provenance
;
np:hasPublicationInfo
dgn-np:NP686047.RASjz8lHwwcnYMkf8Rg4Ighxj3MwdWnfZ07PrOYjhKEa4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP686047.RASjz8lHwwcnYMkf8Rg4Ighxj3MwdWnfZ07PrOYjhKEa4130_assertion
a
np:Assertion
.
dgn-np:NP686047.RASjz8lHwwcnYMkf8Rg4Ighxj3MwdWnfZ07PrOYjhKEa4130_provenance
a
np:Provenance
.
dgn-np:NP686047.RASjz8lHwwcnYMkf8Rg4Ighxj3MwdWnfZ07PrOYjhKEa4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP686047.RASjz8lHwwcnYMkf8Rg4Ighxj3MwdWnfZ07PrOYjhKEa4130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0852654
a
ncit:C7057
.
dgn-gda:DGN207e56a4f3642710f7494da89eea7bbe
sio:SIO_000628
miriam-gene:3630
,
lld:C0852654
;
a
sio:SIO_001121
.
}
dgn-np:NP686047.RASjz8lHwwcnYMkf8Rg4Ighxj3MwdWnfZ07PrOYjhKEa4130_provenance
{
dgn-np:NP686047.RASjz8lHwwcnYMkf8Rg4Ighxj3MwdWnfZ07PrOYjhKEa4130_assertion
dcterms:description
"[A number of physiological alterations in the endocrine milieu at puberty, which include alterations in the growth hormone/insulin-like growth factor axis, insulin sensitivity, as well as the activity of enzymes participating in cortisol metabolism and adrenal steroidogenesis, may account for the documented hypocortisolism and elevated androgen production, and may explain the difficulty in maintaining adequate adrenocortical suppression in pubertal patients with classical 21-hydroxylase deficiency.]. 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:11919101
;
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:NP686047.RASjz8lHwwcnYMkf8Rg4Ighxj3MwdWnfZ07PrOYjhKEa4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:57+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" .
}