@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg
> .
@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:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_head
{
this:
np:hasAssertion
dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_assertion
;
np:hasProvenance
dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_provenance
;
np:hasPublicationInfo
dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_assertion
a
np:Assertion
.
dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_provenance
a
np:Provenance
.
dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_assertion
{
miriam-gene:26121
a
ncit:C16612
.
lld:C0035334
a
ncit:C7057
.
dgn-gda:DGN725d093da63dd34169b130f70d770017
sio:SIO_000628
miriam-gene:26121
,
lld:C0035334
;
a
sio:SIO_001121
.
}
dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_provenance
{
dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_assertion
dcterms:description
"[These findings significantly impact our understanding of the molecular mechanisms underlying RP and suggest that the insufficiency of the functional hPrp31 protein combined with the potential cytotoxicity associated with the expression the AD29 mutant are at least partially causative of the RP phenotype.]. 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:19293337
;
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 .
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dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:16+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
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"v2.1.0" .
}