@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs
> .
@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:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_head
{
this:
np:hasAssertion
dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_assertion
;
np:hasProvenance
dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_provenance
;
np:hasPublicationInfo
dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_assertion
a
np:Assertion
.
dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_provenance
a
np:Provenance
.
dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0520463
a
ncit:C7057
.
dgn-gda:DGNda3c544ac921dce1e74a653f1efbfe9b
sio:SIO_000628
miriam-gene:1756
,
lld:C0520463
;
a
sio:SIO_001121
.
}
dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_provenance
{
dgn-np:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_assertion
dcterms:description
"[This study assessed the clinical and laboratory factors involved in BMD of 45 patients at the Pediatric Unit of Endocrinology, UNICAMP, who had been diagnosed as having classical CAH due to CYP21A2 deficiency including molecular characterization.]. 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:14586796
;
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:NP390083.RAXHS9ipCdO7_7jQtnA5k9cdAuZ6NaK7ikUH2Hqmerqjs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:52+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" .
}