@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP794472.RA9T8ZeoGu2XS_8O63dp5SWsoyEksL1hvc7EBJwfjZzcg
> .
@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:NP794472.RA9T8ZeoGu2XS_8O63dp5SWsoyEksL1hvc7EBJwfjZzcg130_head
{
this:
np:hasAssertion
dgn-np:NP794472.RA9T8ZeoGu2XS_8O63dp5SWsoyEksL1hvc7EBJwfjZzcg130_assertion
;
np:hasProvenance
dgn-np:NP794472.RA9T8ZeoGu2XS_8O63dp5SWsoyEksL1hvc7EBJwfjZzcg130_provenance
;
np:hasPublicationInfo
dgn-np:NP794472.RA9T8ZeoGu2XS_8O63dp5SWsoyEksL1hvc7EBJwfjZzcg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP794472.RA9T8ZeoGu2XS_8O63dp5SWsoyEksL1hvc7EBJwfjZzcg130_assertion
a
np:Assertion
.
dgn-np:NP794472.RA9T8ZeoGu2XS_8O63dp5SWsoyEksL1hvc7EBJwfjZzcg130_provenance
a
np:Provenance
.
dgn-np:NP794472.RA9T8ZeoGu2XS_8O63dp5SWsoyEksL1hvc7EBJwfjZzcg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP794472.RA9T8ZeoGu2XS_8O63dp5SWsoyEksL1hvc7EBJwfjZzcg130_assertion
{
miriam-gene:2070
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGN3ba4be2de17641aa5a486a53b270a4b0
sio:SIO_000628
miriam-gene:2070
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP794472.RA9T8ZeoGu2XS_8O63dp5SWsoyEksL1hvc7EBJwfjZzcg130_provenance
{
dgn-np:NP794472.RA9T8ZeoGu2XS_8O63dp5SWsoyEksL1hvc7EBJwfjZzcg130_assertion
dcterms:description
"[On the basis of these data, the hearing loss phenotype in this American DFNA10 family can be described as postlingual, initially progressive, and resulting, without the influence of presbycusis, in largely stable, flat sensorineural deafness.]. 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:11558763
;
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:NP794472.RA9T8ZeoGu2XS_8O63dp5SWsoyEksL1hvc7EBJwfjZzcg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:08+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" .
}