@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP122280.RARc6agWMVgNb7YK32dSpCGEw-BJgbQkg12JBDnRcq4BY
> .
@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:NP122280.RARc6agWMVgNb7YK32dSpCGEw-BJgbQkg12JBDnRcq4BY130_head
{
this:
np:hasAssertion
dgn-np:NP122280.RARc6agWMVgNb7YK32dSpCGEw-BJgbQkg12JBDnRcq4BY130_assertion
;
np:hasProvenance
dgn-np:NP122280.RARc6agWMVgNb7YK32dSpCGEw-BJgbQkg12JBDnRcq4BY130_provenance
;
np:hasPublicationInfo
dgn-np:NP122280.RARc6agWMVgNb7YK32dSpCGEw-BJgbQkg12JBDnRcq4BY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP122280.RARc6agWMVgNb7YK32dSpCGEw-BJgbQkg12JBDnRcq4BY130_assertion
a
np:Assertion
.
dgn-np:NP122280.RARc6agWMVgNb7YK32dSpCGEw-BJgbQkg12JBDnRcq4BY130_provenance
a
np:Provenance
.
dgn-np:NP122280.RARc6agWMVgNb7YK32dSpCGEw-BJgbQkg12JBDnRcq4BY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP122280.RARc6agWMVgNb7YK32dSpCGEw-BJgbQkg12JBDnRcq4BY130_assertion
{
miriam-gene:10594
a
ncit:C16612
.
lld:C0035334
a
ncit:C7057
.
dgn-gda:DGN0ce9e920c265d419ce68e10209e0f2f6
sio:SIO_000628
miriam-gene:10594
,
lld:C0035334
;
a
sio:SIO_001122
.
}
dgn-np:NP122280.RARc6agWMVgNb7YK32dSpCGEw-BJgbQkg12JBDnRcq4BY130_provenance
{
dgn-np:NP122280.RARc6agWMVgNb7YK32dSpCGEw-BJgbQkg12JBDnRcq4BY130_assertion
dcterms:description
"[The aim of this study was to use lymphoblast cell lines derived from retinitis pigmentosa patients to determine whether mutations in two of these splicing factors, PRPF8 and PRPF31, cause measurable deficiencies in pre-mRNA splicing.]. 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:19096719
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP122280.RARc6agWMVgNb7YK32dSpCGEw-BJgbQkg12JBDnRcq4BY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:03+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" .
}