@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP298812.RAon5DQVpPaZIgXl2j2ssKtoUVX9d3Wl_jYVfb7UxMFPk
> .
@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:NP298812.RAon5DQVpPaZIgXl2j2ssKtoUVX9d3Wl_jYVfb7UxMFPk130_head
{
this:
np:hasAssertion
dgn-np:NP298812.RAon5DQVpPaZIgXl2j2ssKtoUVX9d3Wl_jYVfb7UxMFPk130_assertion
;
np:hasProvenance
dgn-np:NP298812.RAon5DQVpPaZIgXl2j2ssKtoUVX9d3Wl_jYVfb7UxMFPk130_provenance
;
np:hasPublicationInfo
dgn-np:NP298812.RAon5DQVpPaZIgXl2j2ssKtoUVX9d3Wl_jYVfb7UxMFPk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP298812.RAon5DQVpPaZIgXl2j2ssKtoUVX9d3Wl_jYVfb7UxMFPk130_assertion
a
np:Assertion
.
dgn-np:NP298812.RAon5DQVpPaZIgXl2j2ssKtoUVX9d3Wl_jYVfb7UxMFPk130_provenance
a
np:Provenance
.
dgn-np:NP298812.RAon5DQVpPaZIgXl2j2ssKtoUVX9d3Wl_jYVfb7UxMFPk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP298812.RAon5DQVpPaZIgXl2j2ssKtoUVX9d3Wl_jYVfb7UxMFPk130_assertion
{
miriam-gene:3614
a
ncit:C16612
.
lld:C0339525
a
ncit:C7057
.
dgn-gda:DGNd6742ac90cf9ab2152061b99a060de24
sio:SIO_000628
miriam-gene:3614
,
lld:C0339525
;
a
sio:SIO_001121
.
}
dgn-np:NP298812.RAon5DQVpPaZIgXl2j2ssKtoUVX9d3Wl_jYVfb7UxMFPk130_provenance
{
dgn-np:NP298812.RAon5DQVpPaZIgXl2j2ssKtoUVX9d3Wl_jYVfb7UxMFPk130_assertion
dcterms:description
"[To determine the presence and frequency of mutations in the IMPDH1 gene in Japanese patients with autosomal dominant retinitis pigmentosa (ADRP), and to characterize the clinical characteristics of patients with the Lys238Arg mutation in the IMPDH1 gene.]. 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:16038673
;
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:NP298812.RAon5DQVpPaZIgXl2j2ssKtoUVX9d3Wl_jYVfb7UxMFPk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:49+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" .
}