@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1289148.RAOAehGodjgZzIEh_j06ELCn0qTo3_-s2uc6aKop6mMYU
> .
@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:NP1289148.RAOAehGodjgZzIEh_j06ELCn0qTo3_-s2uc6aKop6mMYU130_head
{
this:
np:hasAssertion
dgn-np:NP1289148.RAOAehGodjgZzIEh_j06ELCn0qTo3_-s2uc6aKop6mMYU130_assertion
;
np:hasProvenance
dgn-np:NP1289148.RAOAehGodjgZzIEh_j06ELCn0qTo3_-s2uc6aKop6mMYU130_provenance
;
np:hasPublicationInfo
dgn-np:NP1289148.RAOAehGodjgZzIEh_j06ELCn0qTo3_-s2uc6aKop6mMYU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1289148.RAOAehGodjgZzIEh_j06ELCn0qTo3_-s2uc6aKop6mMYU130_assertion
a
np:Assertion
.
dgn-np:NP1289148.RAOAehGodjgZzIEh_j06ELCn0qTo3_-s2uc6aKop6mMYU130_provenance
a
np:Provenance
.
dgn-np:NP1289148.RAOAehGodjgZzIEh_j06ELCn0qTo3_-s2uc6aKop6mMYU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1289148.RAOAehGodjgZzIEh_j06ELCn0qTo3_-s2uc6aKop6mMYU130_assertion
{
miriam-gene:5566
a
ncit:C16612
.
lld:C0001624
a
ncit:C7057
.
dgn-gda:DGN1bef582d171486f14615e46c35520be9
sio:SIO_000628
miriam-gene:5566
,
lld:C0001624
;
a
sio:SIO_001121
.
}
dgn-np:NP1289148.RAOAehGodjgZzIEh_j06ELCn0qTo3_-s2uc6aKop6mMYU130_provenance
{
dgn-np:NP1289148.RAOAehGodjgZzIEh_j06ELCn0qTo3_-s2uc6aKop6mMYU130_assertion
dcterms:description
"[In this report, we review CNC, its clinical features, diagnosis, treatment and molecular etiology, including PRKAR1A mutations and the newest on PRKACA and PRKACB defects especially as they pertain to adrenal tumors and Cushing's syndrome.]. 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:26130139
;
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:NP1289148.RAOAehGodjgZzIEh_j06ELCn0qTo3_-s2uc6aKop6mMYU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:30+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" .
}