@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP487847.RA-cA1lEGNpyU1mjK4GaCtLmoTIbnDVSIL8loYzRp54W4
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP487847.RA-cA1lEGNpyU1mjK4GaCtLmoTIbnDVSIL8loYzRp54W4130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP487847.RA-cA1lEGNpyU1mjK4GaCtLmoTIbnDVSIL8loYzRp54W4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP487847.RA-cA1lEGNpyU1mjK4GaCtLmoTIbnDVSIL8loYzRp54W4130_assertion
a
np:Assertion
.
dgn-np:NP487847.RA-cA1lEGNpyU1mjK4GaCtLmoTIbnDVSIL8loYzRp54W4130_provenance
a
np:Provenance
.
dgn-np:NP487847.RA-cA1lEGNpyU1mjK4GaCtLmoTIbnDVSIL8loYzRp54W4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP487847.RA-cA1lEGNpyU1mjK4GaCtLmoTIbnDVSIL8loYzRp54W4130_assertion
{
miriam-gene:4627
a
ncit:C16612
.
lld:C1863659
a
ncit:C7057
.
dgn-gda:DGNe323c8bc2cb24a25c1bdda5bf9447eb0
sio:SIO_000628
miriam-gene:4627
,
lld:C1863659
;
a
sio:SIO_001121
.
}
dgn-np:NP487847.RA-cA1lEGNpyU1mjK4GaCtLmoTIbnDVSIL8loYzRp54W4130_provenance
{
dgn-np:NP487847.RA-cA1lEGNpyU1mjK4GaCtLmoTIbnDVSIL8loYzRp54W4130_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:NP487847.RA-cA1lEGNpyU1mjK4GaCtLmoTIbnDVSIL8loYzRp54W4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}