@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP766202.RAtQ3LvYEX3nOjSnIN55kRGOO0DykxmodpjFXA3lRgUcs
> .
@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:NP766202.RAtQ3LvYEX3nOjSnIN55kRGOO0DykxmodpjFXA3lRgUcs130_head
{
this:
np:hasAssertion
dgn-np:NP766202.RAtQ3LvYEX3nOjSnIN55kRGOO0DykxmodpjFXA3lRgUcs130_assertion
;
np:hasProvenance
dgn-np:NP766202.RAtQ3LvYEX3nOjSnIN55kRGOO0DykxmodpjFXA3lRgUcs130_provenance
;
np:hasPublicationInfo
dgn-np:NP766202.RAtQ3LvYEX3nOjSnIN55kRGOO0DykxmodpjFXA3lRgUcs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP766202.RAtQ3LvYEX3nOjSnIN55kRGOO0DykxmodpjFXA3lRgUcs130_assertion
a
np:Assertion
.
dgn-np:NP766202.RAtQ3LvYEX3nOjSnIN55kRGOO0DykxmodpjFXA3lRgUcs130_provenance
a
np:Provenance
.
dgn-np:NP766202.RAtQ3LvYEX3nOjSnIN55kRGOO0DykxmodpjFXA3lRgUcs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP766202.RAtQ3LvYEX3nOjSnIN55kRGOO0DykxmodpjFXA3lRgUcs130_assertion
{
miriam-gene:7399
a
ncit:C16612
.
lld:C0035304
a
ncit:C7057
.
dgn-gda:DGN2331f041e82d4ed166e7ba6424eaf921
sio:SIO_000628
miriam-gene:7399
,
lld:C0035304
;
a
sio:SIO_001121
.
}
dgn-np:NP766202.RAtQ3LvYEX3nOjSnIN55kRGOO0DykxmodpjFXA3lRgUcs130_provenance
{
dgn-np:NP766202.RAtQ3LvYEX3nOjSnIN55kRGOO0DykxmodpjFXA3lRgUcs130_assertion
dcterms:description
"[Patients with USH1 have severe to profound congenital hearing impairment, vestibular dysfunction, and retinal degeneration beginning in childhood, while those with USH2 have moderate to severe hearing impairment, normal vestibular function, and later onset of retinal degeneration.]. 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:10704190
;
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:NP766202.RAtQ3LvYEX3nOjSnIN55kRGOO0DykxmodpjFXA3lRgUcs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:44+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" .
}