@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP323859.RA7gR03MjpXwQ9gWseOdIsexT9dw-FrRzQCUzCjMGRKsE
> .
@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:NP323859.RA7gR03MjpXwQ9gWseOdIsexT9dw-FrRzQCUzCjMGRKsE130_head
{
this:
np:hasAssertion
dgn-np:NP323859.RA7gR03MjpXwQ9gWseOdIsexT9dw-FrRzQCUzCjMGRKsE130_assertion
;
np:hasProvenance
dgn-np:NP323859.RA7gR03MjpXwQ9gWseOdIsexT9dw-FrRzQCUzCjMGRKsE130_provenance
;
np:hasPublicationInfo
dgn-np:NP323859.RA7gR03MjpXwQ9gWseOdIsexT9dw-FrRzQCUzCjMGRKsE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP323859.RA7gR03MjpXwQ9gWseOdIsexT9dw-FrRzQCUzCjMGRKsE130_assertion
a
np:Assertion
.
dgn-np:NP323859.RA7gR03MjpXwQ9gWseOdIsexT9dw-FrRzQCUzCjMGRKsE130_provenance
a
np:Provenance
.
dgn-np:NP323859.RA7gR03MjpXwQ9gWseOdIsexT9dw-FrRzQCUzCjMGRKsE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP323859.RA7gR03MjpXwQ9gWseOdIsexT9dw-FrRzQCUzCjMGRKsE130_assertion
{
miriam-gene:5443
a
ncit:C16612
.
lld:C0206081
a
ncit:C7057
.
dgn-gda:DGN4389e23188ae5e85fee92324f11be5d8
sio:SIO_000628
miriam-gene:5443
,
lld:C0206081
;
a
sio:SIO_001121
.
}
dgn-np:NP323859.RA7gR03MjpXwQ9gWseOdIsexT9dw-FrRzQCUzCjMGRKsE130_provenance
{
dgn-np:NP323859.RA7gR03MjpXwQ9gWseOdIsexT9dw-FrRzQCUzCjMGRKsE130_assertion
dcterms:description
"[We have hypothesized that heterozygosity for CYP21 mutations in women increases their risk of developing clinically evident hyperandrogenism, and that this risk is related to the severity of the mutation of CYP21 and/or the 17-hydroxyprogesterone (17-OHP) response to ACTH stimulation.]. 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:9024240
;
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:NP323859.RA7gR03MjpXwQ9gWseOdIsexT9dw-FrRzQCUzCjMGRKsE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:09+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" .
}