@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP320574.RAcY5muSlEuB9rjVNZAxN51Nf6u5bng_HHe0Gfyco_Y_A
> .
@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:NP320574.RAcY5muSlEuB9rjVNZAxN51Nf6u5bng_HHe0Gfyco_Y_A130_head
{
this:
np:hasAssertion
dgn-np:NP320574.RAcY5muSlEuB9rjVNZAxN51Nf6u5bng_HHe0Gfyco_Y_A130_assertion
;
np:hasProvenance
dgn-np:NP320574.RAcY5muSlEuB9rjVNZAxN51Nf6u5bng_HHe0Gfyco_Y_A130_provenance
;
np:hasPublicationInfo
dgn-np:NP320574.RAcY5muSlEuB9rjVNZAxN51Nf6u5bng_HHe0Gfyco_Y_A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP320574.RAcY5muSlEuB9rjVNZAxN51Nf6u5bng_HHe0Gfyco_Y_A130_assertion
a
np:Assertion
.
dgn-np:NP320574.RAcY5muSlEuB9rjVNZAxN51Nf6u5bng_HHe0Gfyco_Y_A130_provenance
a
np:Provenance
.
dgn-np:NP320574.RAcY5muSlEuB9rjVNZAxN51Nf6u5bng_HHe0Gfyco_Y_A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP320574.RAcY5muSlEuB9rjVNZAxN51Nf6u5bng_HHe0Gfyco_Y_A130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C0001627
a
ncit:C7057
.
dgn-gda:DGN181aff2b811af39ee98233ee635e9dca
sio:SIO_000628
miriam-gene:5972
,
lld:C0001627
;
a
sio:SIO_001121
.
}
dgn-np:NP320574.RAcY5muSlEuB9rjVNZAxN51Nf6u5bng_HHe0Gfyco_Y_A130_provenance
{
dgn-np:NP320574.RAcY5muSlEuB9rjVNZAxN51Nf6u5bng_HHe0Gfyco_Y_A130_assertion
dcterms:description
"[We measured plasma and urinary levels of adrenal hormones, plasma renin activity, and sodium balance longitudinally in the patient and four other patients in whom adrenal hyperplasia had been diagnosed in infancy and in whom DNA analysis had predicted a complete absence of functional P-450c21.]. 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:1984191
;
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:NP320574.RAcY5muSlEuB9rjVNZAxN51Nf6u5bng_HHe0Gfyco_Y_A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:06+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" .
}