@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP126960.RA8oQCrRviDshS9M47mu567FS5uozucsWv-IN0mRYqRA0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP126960.RA8oQCrRviDshS9M47mu567FS5uozucsWv-IN0mRYqRA0130_head
{
this:
np:hasAssertion
dgn-np:NP126960.RA8oQCrRviDshS9M47mu567FS5uozucsWv-IN0mRYqRA0130_assertion
;
np:hasProvenance
dgn-np:NP126960.RA8oQCrRviDshS9M47mu567FS5uozucsWv-IN0mRYqRA0130_provenance
;
np:hasPublicationInfo
dgn-np:NP126960.RA8oQCrRviDshS9M47mu567FS5uozucsWv-IN0mRYqRA0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP126960.RA8oQCrRviDshS9M47mu567FS5uozucsWv-IN0mRYqRA0130_assertion
a
np:Assertion
.
dgn-np:NP126960.RA8oQCrRviDshS9M47mu567FS5uozucsWv-IN0mRYqRA0130_provenance
a
np:Provenance
.
dgn-np:NP126960.RA8oQCrRviDshS9M47mu567FS5uozucsWv-IN0mRYqRA0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP126960.RA8oQCrRviDshS9M47mu567FS5uozucsWv-IN0mRYqRA0130_assertion
{
miriam-gene:7399
a
ncit:C16612
.
lld:C0035334
a
ncit:C7057
.
dgn-gda:DGNad68cbe0e9b82afc1b2849d4e60ebcbb
sio:SIO_000628
miriam-gene:7399
,
lld:C0035334
;
a
sio:SIO_001122
.
}
dgn-np:NP126960.RA8oQCrRviDshS9M47mu567FS5uozucsWv-IN0mRYqRA0130_provenance
{
dgn-np:NP126960.RA8oQCrRviDshS9M47mu567FS5uozucsWv-IN0mRYqRA0130_assertion
dcterms:description
"[Rates of change in patients with the Cys759Phe mutation, the USH2A mutation associated with nonsyndromic disease, were compared with rates of change in patients with the Glu767fs mutation, the most common USH2A mutation associated with Usher syndrome type II (i.e., retinitis pigmentosa and hearing loss).]. 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:18641288
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP126960.RA8oQCrRviDshS9M47mu567FS5uozucsWv-IN0mRYqRA0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:45+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}