@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP362501.RAFrqpdA1alyM6Engs5MxO8DiWXBw4Q85Mjj5HTUIPYRU
> .
@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:NP362501.RAFrqpdA1alyM6Engs5MxO8DiWXBw4Q85Mjj5HTUIPYRU130_head
{
this:
np:hasAssertion
dgn-np:NP362501.RAFrqpdA1alyM6Engs5MxO8DiWXBw4Q85Mjj5HTUIPYRU130_assertion
;
np:hasProvenance
dgn-np:NP362501.RAFrqpdA1alyM6Engs5MxO8DiWXBw4Q85Mjj5HTUIPYRU130_provenance
;
np:hasPublicationInfo
dgn-np:NP362501.RAFrqpdA1alyM6Engs5MxO8DiWXBw4Q85Mjj5HTUIPYRU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP362501.RAFrqpdA1alyM6Engs5MxO8DiWXBw4Q85Mjj5HTUIPYRU130_assertion
a
np:Assertion
.
dgn-np:NP362501.RAFrqpdA1alyM6Engs5MxO8DiWXBw4Q85Mjj5HTUIPYRU130_provenance
a
np:Provenance
.
dgn-np:NP362501.RAFrqpdA1alyM6Engs5MxO8DiWXBw4Q85Mjj5HTUIPYRU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP362501.RAFrqpdA1alyM6Engs5MxO8DiWXBw4Q85Mjj5HTUIPYRU130_assertion
{
miriam-gene:5145
a
ncit:C16612
.
lld:C0035334
a
ncit:C7057
.
dgn-gda:DGN73dc9a131355daf1728ffc46266912f1
sio:SIO_000628
miriam-gene:5145
,
lld:C0035334
;
a
sio:SIO_001121
.
}
dgn-np:NP362501.RAFrqpdA1alyM6Engs5MxO8DiWXBw4Q85Mjj5HTUIPYRU130_provenance
{
dgn-np:NP362501.RAFrqpdA1alyM6Engs5MxO8DiWXBw4Q85Mjj5HTUIPYRU130_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_literature
;
sio:SIO_000772
miriam-pubmed:7493036
;
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:NP362501.RAFrqpdA1alyM6Engs5MxO8DiWXBw4Q85Mjj5HTUIPYRU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:32+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" .
}