@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP389588.RAJSxcGs99bsR-fQmDv1kp82AQYsz2d452F8VRDBnH2KA
> .
@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:NP389588.RAJSxcGs99bsR-fQmDv1kp82AQYsz2d452F8VRDBnH2KA130_head
{
this:
np:hasAssertion
dgn-np:NP389588.RAJSxcGs99bsR-fQmDv1kp82AQYsz2d452F8VRDBnH2KA130_assertion
;
np:hasProvenance
dgn-np:NP389588.RAJSxcGs99bsR-fQmDv1kp82AQYsz2d452F8VRDBnH2KA130_provenance
;
np:hasPublicationInfo
dgn-np:NP389588.RAJSxcGs99bsR-fQmDv1kp82AQYsz2d452F8VRDBnH2KA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP389588.RAJSxcGs99bsR-fQmDv1kp82AQYsz2d452F8VRDBnH2KA130_assertion
a
np:Assertion
.
dgn-np:NP389588.RAJSxcGs99bsR-fQmDv1kp82AQYsz2d452F8VRDBnH2KA130_provenance
a
np:Provenance
.
dgn-np:NP389588.RAJSxcGs99bsR-fQmDv1kp82AQYsz2d452F8VRDBnH2KA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP389588.RAJSxcGs99bsR-fQmDv1kp82AQYsz2d452F8VRDBnH2KA130_assertion
{
miriam-gene:80207
a
ncit:C16612
.
lld:C0018784
a
ncit:C7057
.
dgn-gda:DGN040ed6d9759ef4d2b9aa26609c94c07c
sio:SIO_000628
miriam-gene:80207
,
lld:C0018784
;
a
sio:SIO_001121
.
}
dgn-np:NP389588.RAJSxcGs99bsR-fQmDv1kp82AQYsz2d452F8VRDBnH2KA130_provenance
{
dgn-np:NP389588.RAJSxcGs99bsR-fQmDv1kp82AQYsz2d452F8VRDBnH2KA130_assertion
dcterms:description
"[Linkage and sequence mutation analyses of the ADOA candidate genes OPA1, OPA3, OPA4, and OPA5, including the genes WFS1, GJB2, and GJB6 associated with recessive inherited OA or dominant LFSNHL, were performed.]. 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:16648378
;
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:NP389588.RAJSxcGs99bsR-fQmDv1kp82AQYsz2d452F8VRDBnH2KA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:52+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" .
}