@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP590397.RAbHBBsiW_bpNE9tEWdnyhHpor-exVtb3EfGtRzPMLepQ
> .
@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:NP590397.RAbHBBsiW_bpNE9tEWdnyhHpor-exVtb3EfGtRzPMLepQ130_head
{
this:
np:hasAssertion
dgn-np:NP590397.RAbHBBsiW_bpNE9tEWdnyhHpor-exVtb3EfGtRzPMLepQ130_assertion
;
np:hasProvenance
dgn-np:NP590397.RAbHBBsiW_bpNE9tEWdnyhHpor-exVtb3EfGtRzPMLepQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP590397.RAbHBBsiW_bpNE9tEWdnyhHpor-exVtb3EfGtRzPMLepQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP590397.RAbHBBsiW_bpNE9tEWdnyhHpor-exVtb3EfGtRzPMLepQ130_assertion
a
np:Assertion
.
dgn-np:NP590397.RAbHBBsiW_bpNE9tEWdnyhHpor-exVtb3EfGtRzPMLepQ130_provenance
a
np:Provenance
.
dgn-np:NP590397.RAbHBBsiW_bpNE9tEWdnyhHpor-exVtb3EfGtRzPMLepQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP590397.RAbHBBsiW_bpNE9tEWdnyhHpor-exVtb3EfGtRzPMLepQ130_assertion
{
miriam-gene:5573
a
ncit:C16612
.
lld:C1857451
a
ncit:C7057
.
dgn-gda:DGNed93f9b10801c32ed34539e2835d0dff
sio:SIO_000628
miriam-gene:5573
,
lld:C1857451
;
a
sio:SIO_001121
.
}
dgn-np:NP590397.RAbHBBsiW_bpNE9tEWdnyhHpor-exVtb3EfGtRzPMLepQ130_provenance
{
dgn-np:NP590397.RAbHBBsiW_bpNE9tEWdnyhHpor-exVtb3EfGtRzPMLepQ130_assertion
dcterms:description
"[Somatic and germ line inactivating mutations of PRKAR1 (regulatory subunit R1A of PKA) can be observed in patient with isolated primary pigmented nodular adrenocortical disease (PPNAD) and AA responsible for ACS.]. 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:12530696
;
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:NP590397.RAbHBBsiW_bpNE9tEWdnyhHpor-exVtb3EfGtRzPMLepQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:55+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" .
}