@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP496872.RAIBxElqE1felAydFc4N3HKbeRTbT4ycdeRh30--T3Km8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP496872.RAIBxElqE1felAydFc4N3HKbeRTbT4ycdeRh30--T3Km8130_head
{
this:
np:hasAssertion
dgn-np:NP496872.RAIBxElqE1felAydFc4N3HKbeRTbT4ycdeRh30--T3Km8130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP496872.RAIBxElqE1felAydFc4N3HKbeRTbT4ycdeRh30--T3Km8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP496872.RAIBxElqE1felAydFc4N3HKbeRTbT4ycdeRh30--T3Km8130_assertion
a
np:Assertion
.
dgn-np:NP496872.RAIBxElqE1felAydFc4N3HKbeRTbT4ycdeRh30--T3Km8130_provenance
a
np:Provenance
.
dgn-np:NP496872.RAIBxElqE1felAydFc4N3HKbeRTbT4ycdeRh30--T3Km8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP496872.RAIBxElqE1felAydFc4N3HKbeRTbT4ycdeRh30--T3Km8130_assertion
{
miriam-gene:5573
a
ncit:C16612
.
lld:C0151468
a
ncit:C7057
.
dgn-gda:DGNdedfda1c4f3ace43520aee7f44461829
sio:SIO_000628
miriam-gene:5573
,
lld:C0151468
;
a
sio:SIO_001122
.
}
dgn-np:NP496872.RAIBxElqE1felAydFc4N3HKbeRTbT4ycdeRh30--T3Km8130_provenance
{
dgn-np:NP496872.RAIBxElqE1felAydFc4N3HKbeRTbT4ycdeRh30--T3Km8130_assertion
dcterms:description
"[Heterozygous loss of function mutations in human PKAR1A gene (PRKAR1A) have been identified in patients with Carney complex (CNC), an autosomal dominant familial multiple neoplasia syndrome displaying different endocrine tumors, including adrenocortical tumors, GH-secreting pituitary tumors and thyroid adenomas.]. 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:15921845
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP496872.RAIBxElqE1felAydFc4N3HKbeRTbT4ycdeRh30--T3Km8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:30+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}