@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8
> .
@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:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_head
{
this:
np:hasAssertion
dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_assertion
;
np:hasProvenance
dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_provenance
;
np:hasPublicationInfo
dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_assertion
a
np:Assertion
.
dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_provenance
a
np:Provenance
.
dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_assertion
{
miriam-gene:1583
a
ncit:C16612
.
lld:C0342492
a
ncit:C7057
.
dgn-gda:DGN7618fdbe233c8ca2da34ec685be0b5cf
sio:SIO_000628
miriam-gene:1583
,
lld:C0342492
;
a
sio:SIO_001121
.
}
dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_provenance
{
dgn-np:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_assertion
dcterms:description
"[These studies show that lipoid CAH is not caused by lesions in the P450scc gene, and suggest that another unidentified factor is required for the conversion of cholesterol to pregnenolone, and is disordered in congenital lipoid adrenal hyperplasia.]. 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:1661294
;
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:NP420745.RAK0bbLC6jDRE_Cv0758a1V38eSqFdihLPIuwdDlhj7r8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:09+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" .
}