@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP537186.RAsBq9pkAxAjfoMx-Q85QrQXLZiFI6deq9TC74heIMkxQ
> .
@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:NP537186.RAsBq9pkAxAjfoMx-Q85QrQXLZiFI6deq9TC74heIMkxQ130_head
{
this:
np:hasAssertion
dgn-np:NP537186.RAsBq9pkAxAjfoMx-Q85QrQXLZiFI6deq9TC74heIMkxQ130_assertion
;
np:hasProvenance
dgn-np:NP537186.RAsBq9pkAxAjfoMx-Q85QrQXLZiFI6deq9TC74heIMkxQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP537186.RAsBq9pkAxAjfoMx-Q85QrQXLZiFI6deq9TC74heIMkxQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP537186.RAsBq9pkAxAjfoMx-Q85QrQXLZiFI6deq9TC74heIMkxQ130_assertion
a
np:Assertion
.
dgn-np:NP537186.RAsBq9pkAxAjfoMx-Q85QrQXLZiFI6deq9TC74heIMkxQ130_provenance
a
np:Provenance
.
dgn-np:NP537186.RAsBq9pkAxAjfoMx-Q85QrQXLZiFI6deq9TC74heIMkxQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP537186.RAsBq9pkAxAjfoMx-Q85QrQXLZiFI6deq9TC74heIMkxQ130_assertion
{
miriam-gene:50940
a
ncit:C16612
.
lld:C1336708
a
ncit:C7057
.
dgn-gda:DGNb76ef34ff0ad81e4dea0e4e728899662
sio:SIO_000628
miriam-gene:50940
,
lld:C1336708
;
a
sio:SIO_001121
.
}
dgn-np:NP537186.RAsBq9pkAxAjfoMx-Q85QrQXLZiFI6deq9TC74heIMkxQ130_provenance
{
dgn-np:NP537186.RAsBq9pkAxAjfoMx-Q85QrQXLZiFI6deq9TC74heIMkxQ130_assertion
dcterms:description
"[Most variants were detected in the general population, but functional studies showed that all these mutations reduced PDE activity, and that PDE11A protein expression was decreased (or absent) in TGCT samples from carriers.]. 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:19549888
;
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:NP537186.RAsBq9pkAxAjfoMx-Q85QrQXLZiFI6deq9TC74heIMkxQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:24+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" .
}