@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP487963.RAXsShH8hfeOG7vgYmhiULkcBD3XeMz7a5oF-f4S1YSo8
> .
@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:NP487963.RAXsShH8hfeOG7vgYmhiULkcBD3XeMz7a5oF-f4S1YSo8130_head
{
this:
np:hasAssertion
dgn-np:NP487963.RAXsShH8hfeOG7vgYmhiULkcBD3XeMz7a5oF-f4S1YSo8130_assertion
;
np:hasProvenance
dgn-np:NP487963.RAXsShH8hfeOG7vgYmhiULkcBD3XeMz7a5oF-f4S1YSo8130_provenance
;
np:hasPublicationInfo
dgn-np:NP487963.RAXsShH8hfeOG7vgYmhiULkcBD3XeMz7a5oF-f4S1YSo8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP487963.RAXsShH8hfeOG7vgYmhiULkcBD3XeMz7a5oF-f4S1YSo8130_assertion
a
np:Assertion
.
dgn-np:NP487963.RAXsShH8hfeOG7vgYmhiULkcBD3XeMz7a5oF-f4S1YSo8130_provenance
a
np:Provenance
.
dgn-np:NP487963.RAXsShH8hfeOG7vgYmhiULkcBD3XeMz7a5oF-f4S1YSo8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP487963.RAXsShH8hfeOG7vgYmhiULkcBD3XeMz7a5oF-f4S1YSo8130_assertion
{
miriam-gene:1589
a
ncit:C16612
.
lld:C0206081
a
ncit:C7057
.
dgn-gda:DGNa2b272908647386cfd3be9d325f43667
sio:SIO_000628
miriam-gene:1589
,
lld:C0206081
;
a
sio:SIO_001121
.
}
dgn-np:NP487963.RAXsShH8hfeOG7vgYmhiULkcBD3XeMz7a5oF-f4S1YSo8130_provenance
{
dgn-np:NP487963.RAXsShH8hfeOG7vgYmhiULkcBD3XeMz7a5oF-f4S1YSo8130_assertion
dcterms:description
"[Four patients (three with idiopathic hirsutism, one with ovarian hyperandrogenism) and one control were carriers of CYP21 mutations typically associated with classic congenital adrenal hyperplasia but had normal basal and ACTH-stimulated 17-hydroxyprogesterone levels.]. 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:10521100
;
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:NP487963.RAXsShH8hfeOG7vgYmhiULkcBD3XeMz7a5oF-f4S1YSo8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}