@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP520856.RAgUGL-WVyBjxds8iOjYAUl59-JuFRlt5U5PjHEPQ58AQ
> .
@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:NP520856.RAgUGL-WVyBjxds8iOjYAUl59-JuFRlt5U5PjHEPQ58AQ130_head
{
this:
np:hasAssertion
dgn-np:NP520856.RAgUGL-WVyBjxds8iOjYAUl59-JuFRlt5U5PjHEPQ58AQ130_assertion
;
np:hasProvenance
dgn-np:NP520856.RAgUGL-WVyBjxds8iOjYAUl59-JuFRlt5U5PjHEPQ58AQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP520856.RAgUGL-WVyBjxds8iOjYAUl59-JuFRlt5U5PjHEPQ58AQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP520856.RAgUGL-WVyBjxds8iOjYAUl59-JuFRlt5U5PjHEPQ58AQ130_assertion
a
np:Assertion
.
dgn-np:NP520856.RAgUGL-WVyBjxds8iOjYAUl59-JuFRlt5U5PjHEPQ58AQ130_provenance
a
np:Provenance
.
dgn-np:NP520856.RAgUGL-WVyBjxds8iOjYAUl59-JuFRlt5U5PjHEPQ58AQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP520856.RAgUGL-WVyBjxds8iOjYAUl59-JuFRlt5U5PjHEPQ58AQ130_assertion
{
miriam-gene:5741
a
ncit:C16612
.
lld:C0410528
a
ncit:C7057
.
dgn-gda:DGN728500cdb73e803144857f1eeadb4044
sio:SIO_000628
miriam-gene:5741
,
lld:C0410528
;
a
sio:SIO_001121
.
}
dgn-np:NP520856.RAgUGL-WVyBjxds8iOjYAUl59-JuFRlt5U5PjHEPQ58AQ130_provenance
{
dgn-np:NP520856.RAgUGL-WVyBjxds8iOjYAUl59-JuFRlt5U5PjHEPQ58AQ130_assertion
dcterms:description
"[Recently, however, mutations in PRKAR1A, a regulatory subunit of the cAMP-dependent protein kinase, have been identified in several cases of PTH and other hormone resistance and skeletal dysplasia that are considered to be affected by PHP type II due to unimpaired urinary excretion of cAMP following PTH administration.]. 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:23392091
;
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:NP520856.RAgUGL-WVyBjxds8iOjYAUl59-JuFRlt5U5PjHEPQ58AQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:10+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" .
}