@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g
> .
@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:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_head
{
this:
np:hasAssertion
dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_assertion
;
np:hasProvenance
dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_provenance
;
np:hasPublicationInfo
dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_assertion
a
np:Assertion
.
dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_provenance
a
np:Provenance
.
dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_assertion
{
miriam-gene:54567
a
ncit:C16612
.
lld:C1291601
a
ncit:C7057
.
dgn-gda:DGNdc2b850200eb99bd740133853324f1b1
sio:SIO_000628
miriam-gene:54567
,
lld:C1291601
;
a
sio:SIO_001121
.
}
dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_provenance
{
dgn-np:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_assertion
dcterms:description
"[Nonclassical 3 beta-hydroxysteroid dehydrogenase/delta 5-delta 4-isomerase deficiency (NC3 beta HSDD) has been diagnosed in hyperandrogenic women with an increasing frequency during the last 14 yr. Fifteen menarcheal women with androgen excess syndrome, diagnosed with NC3 beta HSDD previously were restudied, in 12 after discontinuation of glucocorticoid treatment, in 2 patients never treated with glucocorticoids, and in 1 both before and after glucocorticoid therapy.]. 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:7989489
;
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:NP767907.RAucpcnZyX5lodNK25osl6wh_4AFnDXr_gfupQfFuoV6g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:44+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" .
}