@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP4831.RA0eUcwmkCeLfw6howRNTHrPxMBHyPrgIb4tLTeqcsKsw
> .
@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:NP4831.RA0eUcwmkCeLfw6howRNTHrPxMBHyPrgIb4tLTeqcsKsw130_head
{
this:
np:hasAssertion
dgn-np:NP4831.RA0eUcwmkCeLfw6howRNTHrPxMBHyPrgIb4tLTeqcsKsw130_assertion
;
np:hasProvenance
dgn-np:NP4831.RA0eUcwmkCeLfw6howRNTHrPxMBHyPrgIb4tLTeqcsKsw130_provenance
;
np:hasPublicationInfo
dgn-np:NP4831.RA0eUcwmkCeLfw6howRNTHrPxMBHyPrgIb4tLTeqcsKsw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP4831.RA0eUcwmkCeLfw6howRNTHrPxMBHyPrgIb4tLTeqcsKsw130_assertion
a
np:Assertion
.
dgn-np:NP4831.RA0eUcwmkCeLfw6howRNTHrPxMBHyPrgIb4tLTeqcsKsw130_provenance
a
np:Provenance
.
dgn-np:NP4831.RA0eUcwmkCeLfw6howRNTHrPxMBHyPrgIb4tLTeqcsKsw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP4831.RA0eUcwmkCeLfw6howRNTHrPxMBHyPrgIb4tLTeqcsKsw130_assertion
{
miriam-gene:5145
a
ncit:C16612
.
lld:C3151139
a
ncit:C7057
.
dgn-gda:DGN2324c3a615324f44c3e1b227b7870e7f
sio:SIO_000628
miriam-gene:5145
,
lld:C3151139
;
a
sio:SIO_001122
.
}
dgn-np:NP4831.RA0eUcwmkCeLfw6howRNTHrPxMBHyPrgIb4tLTeqcsKsw130_provenance
{
dgn-np:NP4831.RA0eUcwmkCeLfw6howRNTHrPxMBHyPrgIb4tLTeqcsKsw130_assertion
dcterms:description
"[As null mutations in PDEB cause some cases of RP and since both alpha and beta subunits are required for full phosphodiesterase activity, we examined the gene encoding the alpha subunit of cGMP phosphodiesterase (PDEA) in 340 unrelated patients with RP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:7493036
;
prov:wasDerivedFrom
dgn-void:uniprot-20130724
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
dgn-void:uniprot-20130724
pav:importedOn
"2013-07-24"^^
xsd:date
.
}
dgn-np:NP4831.RA0eUcwmkCeLfw6howRNTHrPxMBHyPrgIb4tLTeqcsKsw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:00+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" .
}