@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP652802.RAuxIRd5OwCqyIvu7GwkNvUEBWoO7_kwO0PvcYZdkmYvg
> .
@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:NP652802.RAuxIRd5OwCqyIvu7GwkNvUEBWoO7_kwO0PvcYZdkmYvg130_head
{
this:
np:hasAssertion
dgn-np:NP652802.RAuxIRd5OwCqyIvu7GwkNvUEBWoO7_kwO0PvcYZdkmYvg130_assertion
;
np:hasProvenance
dgn-np:NP652802.RAuxIRd5OwCqyIvu7GwkNvUEBWoO7_kwO0PvcYZdkmYvg130_provenance
;
np:hasPublicationInfo
dgn-np:NP652802.RAuxIRd5OwCqyIvu7GwkNvUEBWoO7_kwO0PvcYZdkmYvg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP652802.RAuxIRd5OwCqyIvu7GwkNvUEBWoO7_kwO0PvcYZdkmYvg130_assertion
a
np:Assertion
.
dgn-np:NP652802.RAuxIRd5OwCqyIvu7GwkNvUEBWoO7_kwO0PvcYZdkmYvg130_provenance
a
np:Provenance
.
dgn-np:NP652802.RAuxIRd5OwCqyIvu7GwkNvUEBWoO7_kwO0PvcYZdkmYvg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP652802.RAuxIRd5OwCqyIvu7GwkNvUEBWoO7_kwO0PvcYZdkmYvg130_assertion
{
miriam-gene:6770
a
ncit:C16612
.
lld:C0405580
a
ncit:C7057
.
dgn-gda:DGN0f2c213062f55865dee63d9898dbddff
sio:SIO_000628
miriam-gene:6770
,
lld:C0405580
;
a
sio:SIO_001121
.
}
dgn-np:NP652802.RAuxIRd5OwCqyIvu7GwkNvUEBWoO7_kwO0PvcYZdkmYvg130_provenance
{
dgn-np:NP652802.RAuxIRd5OwCqyIvu7GwkNvUEBWoO7_kwO0PvcYZdkmYvg130_assertion
dcterms:description
"[Congenital lipoid adrenal hyperplasia is an autosomal recessive condition due to mutations in Steroidogenic Acute Regulatory Protein (StAR) associated with the inability to synthesize all adrenal and gonadal steroids, resulting in adrenal insufficiency and failure to develop male genitalia in affected 46,XY 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:18058976
;
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:NP652802.RAuxIRd5OwCqyIvu7GwkNvUEBWoO7_kwO0PvcYZdkmYvg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:33+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" .
}