@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP684365.RAc_Tk9d9U5H7i_SCH6mkbkxEf6gep5B3oh9NIU24Fx54
> .
@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:NP684365.RAc_Tk9d9U5H7i_SCH6mkbkxEf6gep5B3oh9NIU24Fx54130_head
{
this:
np:hasAssertion
dgn-np:NP684365.RAc_Tk9d9U5H7i_SCH6mkbkxEf6gep5B3oh9NIU24Fx54130_assertion
;
np:hasProvenance
dgn-np:NP684365.RAc_Tk9d9U5H7i_SCH6mkbkxEf6gep5B3oh9NIU24Fx54130_provenance
;
np:hasPublicationInfo
dgn-np:NP684365.RAc_Tk9d9U5H7i_SCH6mkbkxEf6gep5B3oh9NIU24Fx54130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP684365.RAc_Tk9d9U5H7i_SCH6mkbkxEf6gep5B3oh9NIU24Fx54130_assertion
a
np:Assertion
.
dgn-np:NP684365.RAc_Tk9d9U5H7i_SCH6mkbkxEf6gep5B3oh9NIU24Fx54130_provenance
a
np:Provenance
.
dgn-np:NP684365.RAc_Tk9d9U5H7i_SCH6mkbkxEf6gep5B3oh9NIU24Fx54130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP684365.RAc_Tk9d9U5H7i_SCH6mkbkxEf6gep5B3oh9NIU24Fx54130_assertion
{
miriam-gene:5443
a
ncit:C16612
.
lld:C1621895
a
ncit:C7057
.
dgn-gda:DGNd371ab4b9d3af6cc58ee57ea2244b830
sio:SIO_000628
miriam-gene:5443
,
lld:C1621895
;
a
sio:SIO_001121
.
}
dgn-np:NP684365.RAc_Tk9d9U5H7i_SCH6mkbkxEf6gep5B3oh9NIU24Fx54130_provenance
{
dgn-np:NP684365.RAc_Tk9d9U5H7i_SCH6mkbkxEf6gep5B3oh9NIU24Fx54130_assertion
dcterms:description
"[The hormonal responses to ACTH of the family members with cryptic 21-hydroxylase deficiency were determined and compared to the responses of patients with CAH, patients with acquired adrenal hyperplasia, family members predicted to be heterozygous for CAH, family members predicted to be unaffected, and the general population.]. 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:6271801
;
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:NP684365.RAc_Tk9d9U5H7i_SCH6mkbkxEf6gep5B3oh9NIU24Fx54130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:56+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" .
}