@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP663811.RAIoaNlHRYaa3R0VH6U0OXPc_nx_OMYtpwICp5uKmbBKk
> .
@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:NP663811.RAIoaNlHRYaa3R0VH6U0OXPc_nx_OMYtpwICp5uKmbBKk130_head
{
this:
np:hasAssertion
dgn-np:NP663811.RAIoaNlHRYaa3R0VH6U0OXPc_nx_OMYtpwICp5uKmbBKk130_assertion
;
np:hasProvenance
dgn-np:NP663811.RAIoaNlHRYaa3R0VH6U0OXPc_nx_OMYtpwICp5uKmbBKk130_provenance
;
np:hasPublicationInfo
dgn-np:NP663811.RAIoaNlHRYaa3R0VH6U0OXPc_nx_OMYtpwICp5uKmbBKk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP663811.RAIoaNlHRYaa3R0VH6U0OXPc_nx_OMYtpwICp5uKmbBKk130_assertion
a
np:Assertion
.
dgn-np:NP663811.RAIoaNlHRYaa3R0VH6U0OXPc_nx_OMYtpwICp5uKmbBKk130_provenance
a
np:Provenance
.
dgn-np:NP663811.RAIoaNlHRYaa3R0VH6U0OXPc_nx_OMYtpwICp5uKmbBKk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP663811.RAIoaNlHRYaa3R0VH6U0OXPc_nx_OMYtpwICp5uKmbBKk130_assertion
{
miriam-gene:5573
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGNfe49a6643b704a006d712b2ef5c78739
sio:SIO_000628
miriam-gene:5573
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP663811.RAIoaNlHRYaa3R0VH6U0OXPc_nx_OMYtpwICp5uKmbBKk130_provenance
{
dgn-np:NP663811.RAIoaNlHRYaa3R0VH6U0OXPc_nx_OMYtpwICp5uKmbBKk130_assertion
dcterms:description
"[Finally, Carney complex, which affects the adrenal cortex, the pituitary and thyroid glands, and the gonads, is caused by mutations in the gene that codes for regulatory subunit type 1A of protein kinase A (PKA) (PRKAR1A) in at least half of the known patients.]. 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:11407658
;
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:NP663811.RAIoaNlHRYaa3R0VH6U0OXPc_nx_OMYtpwICp5uKmbBKk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:41+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" .
}