@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP911963.RAzKrqMkK6ROx0JlfOm9-VDEgIW-a07Y2iETTwMXfUh9s
> .
@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:NP911963.RAzKrqMkK6ROx0JlfOm9-VDEgIW-a07Y2iETTwMXfUh9s130_head
{
this:
np:hasAssertion
dgn-np:NP911963.RAzKrqMkK6ROx0JlfOm9-VDEgIW-a07Y2iETTwMXfUh9s130_assertion
;
np:hasProvenance
dgn-np:NP911963.RAzKrqMkK6ROx0JlfOm9-VDEgIW-a07Y2iETTwMXfUh9s130_provenance
;
np:hasPublicationInfo
dgn-np:NP911963.RAzKrqMkK6ROx0JlfOm9-VDEgIW-a07Y2iETTwMXfUh9s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP911963.RAzKrqMkK6ROx0JlfOm9-VDEgIW-a07Y2iETTwMXfUh9s130_assertion
a
np:Assertion
.
dgn-np:NP911963.RAzKrqMkK6ROx0JlfOm9-VDEgIW-a07Y2iETTwMXfUh9s130_provenance
a
np:Provenance
.
dgn-np:NP911963.RAzKrqMkK6ROx0JlfOm9-VDEgIW-a07Y2iETTwMXfUh9s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP911963.RAzKrqMkK6ROx0JlfOm9-VDEgIW-a07Y2iETTwMXfUh9s130_assertion
{
miriam-gene:7393
a
ncit:C16612
.
lld:C0154823
a
ncit:C7057
.
dgn-gda:DGNb4f59e3bc8c577cdf24858216ba0c266
sio:SIO_000628
miriam-gene:7393
,
lld:C0154823
;
a
sio:SIO_001121
.
}
dgn-np:NP911963.RAzKrqMkK6ROx0JlfOm9-VDEgIW-a07Y2iETTwMXfUh9s130_provenance
{
dgn-np:NP911963.RAzKrqMkK6ROx0JlfOm9-VDEgIW-a07Y2iETTwMXfUh9s130_assertion
dcterms:description
"[Whereas the mechanisms underlying hearing impairment in USH patients are being unraveled, showing in particular that USH1 proteins are involved in the shaping of the hair bundle and the functioning of the mechanoelectrical transduction machinery, the mechanisms underlying the retinal defects are still unclear.]. 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:22185901
;
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:NP911963.RAzKrqMkK6ROx0JlfOm9-VDEgIW-a07Y2iETTwMXfUh9s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:19+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" .
}