@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP385322.RAd3KnXujCZ6KpJ1qRQHyXvU9IphCU7HqwtOTrtK4rV-g
> .
@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:NP385322.RAd3KnXujCZ6KpJ1qRQHyXvU9IphCU7HqwtOTrtK4rV-g130_head
{
this:
np:hasAssertion
dgn-np:NP385322.RAd3KnXujCZ6KpJ1qRQHyXvU9IphCU7HqwtOTrtK4rV-g130_assertion
;
np:hasProvenance
dgn-np:NP385322.RAd3KnXujCZ6KpJ1qRQHyXvU9IphCU7HqwtOTrtK4rV-g130_provenance
;
np:hasPublicationInfo
dgn-np:NP385322.RAd3KnXujCZ6KpJ1qRQHyXvU9IphCU7HqwtOTrtK4rV-g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP385322.RAd3KnXujCZ6KpJ1qRQHyXvU9IphCU7HqwtOTrtK4rV-g130_assertion
a
np:Assertion
.
dgn-np:NP385322.RAd3KnXujCZ6KpJ1qRQHyXvU9IphCU7HqwtOTrtK4rV-g130_provenance
a
np:Provenance
.
dgn-np:NP385322.RAd3KnXujCZ6KpJ1qRQHyXvU9IphCU7HqwtOTrtK4rV-g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP385322.RAd3KnXujCZ6KpJ1qRQHyXvU9IphCU7HqwtOTrtK4rV-g130_assertion
{
miriam-gene:4627
a
ncit:C16612
.
lld:C1861512
a
ncit:C7057
.
dgn-gda:DGNfea3661ce242fee03d96fba5f4164228
sio:SIO_000628
miriam-gene:4627
,
lld:C1861512
;
a
sio:SIO_001121
.
}
dgn-np:NP385322.RAd3KnXujCZ6KpJ1qRQHyXvU9IphCU7HqwtOTrtK4rV-g130_provenance
{
dgn-np:NP385322.RAd3KnXujCZ6KpJ1qRQHyXvU9IphCU7HqwtOTrtK4rV-g130_assertion
dcterms:description
"[Both the precise role of MYH9 in the cochlea and the mechanism by which the R705H mutation leads to the DFNA17 phenotype (progressive hearing impairment and cochleosaccular degeneration) remain to be elucidated.]. 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:11023810
;
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:NP385322.RAd3KnXujCZ6KpJ1qRQHyXvU9IphCU7HqwtOTrtK4rV-g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:49+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" .
}