@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP357023.RAdU2StD-GZ2zoN0Lc9EYUPQ4N6otimOYntwylAH8BEeo
> .
@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/v4.0.0/void/
> .
dgn-np:NP357023.RAdU2StD-GZ2zoN0Lc9EYUPQ4N6otimOYntwylAH8BEeo130_head
{
this:
np:hasAssertion
dgn-np:NP357023.RAdU2StD-GZ2zoN0Lc9EYUPQ4N6otimOYntwylAH8BEeo130_assertion
;
np:hasProvenance
dgn-np:NP357023.RAdU2StD-GZ2zoN0Lc9EYUPQ4N6otimOYntwylAH8BEeo130_provenance
;
np:hasPublicationInfo
dgn-np:NP357023.RAdU2StD-GZ2zoN0Lc9EYUPQ4N6otimOYntwylAH8BEeo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP357023.RAdU2StD-GZ2zoN0Lc9EYUPQ4N6otimOYntwylAH8BEeo130_assertion
a
np:Assertion
.
dgn-np:NP357023.RAdU2StD-GZ2zoN0Lc9EYUPQ4N6otimOYntwylAH8BEeo130_provenance
a
np:Provenance
.
dgn-np:NP357023.RAdU2StD-GZ2zoN0Lc9EYUPQ4N6otimOYntwylAH8BEeo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP357023.RAdU2StD-GZ2zoN0Lc9EYUPQ4N6otimOYntwylAH8BEeo130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0158687
a
ncit:C7057
.
dgn-gda:DGN3d93cbc28c5fd81f4ebc4bd243991779
sio:SIO_000628
miriam-gene:367
,
lld:C0158687
;
a
sio:SIO_001122
.
}
dgn-np:NP357023.RAdU2StD-GZ2zoN0Lc9EYUPQ4N6otimOYntwylAH8BEeo130_provenance
{
dgn-np:NP357023.RAdU2StD-GZ2zoN0Lc9EYUPQ4N6otimOYntwylAH8BEeo130_assertion
dcterms:description
"[We conclude that AR gene mutations or polymorphisms are not a common factor influencing the degree of hyperandrogenic symptoms displayed by CAH girls, and that the AR E653K mutation is compatible with normal genital development, although it can cause genital malformations in susceptible individuals.]. 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:12050225
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP357023.RAdU2StD-GZ2zoN0Lc9EYUPQ4N6otimOYntwylAH8BEeo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:27+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}