@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1074119.RAkiKWi8EDc3jgmUjOHnJ_ch-qL9Nn6hRE0EpaOW8Qa1Y
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1074119.RAkiKWi8EDc3jgmUjOHnJ_ch-qL9Nn6hRE0EpaOW8Qa1Y130_head
{
this:
np:hasAssertion
dgn-np:NP1074119.RAkiKWi8EDc3jgmUjOHnJ_ch-qL9Nn6hRE0EpaOW8Qa1Y130_assertion
;
np:hasProvenance
dgn-np:NP1074119.RAkiKWi8EDc3jgmUjOHnJ_ch-qL9Nn6hRE0EpaOW8Qa1Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP1074119.RAkiKWi8EDc3jgmUjOHnJ_ch-qL9Nn6hRE0EpaOW8Qa1Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1074119.RAkiKWi8EDc3jgmUjOHnJ_ch-qL9Nn6hRE0EpaOW8Qa1Y130_assertion
a
np:Assertion
.
dgn-np:NP1074119.RAkiKWi8EDc3jgmUjOHnJ_ch-qL9Nn6hRE0EpaOW8Qa1Y130_provenance
a
np:Provenance
.
dgn-np:NP1074119.RAkiKWi8EDc3jgmUjOHnJ_ch-qL9Nn6hRE0EpaOW8Qa1Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1074119.RAkiKWi8EDc3jgmUjOHnJ_ch-qL9Nn6hRE0EpaOW8Qa1Y130_assertion
{
miriam-gene:4646
a
ncit:C16612
.
lld:C0155552
a
ncit:C7057
.
dgn-gda:DGN117f81f16a12d1f331460cea122c082e
sio:SIO_000628
miriam-gene:4646
,
lld:C0155552
;
a
sio:SIO_001121
.
}
dgn-np:NP1074119.RAkiKWi8EDc3jgmUjOHnJ_ch-qL9Nn6hRE0EpaOW8Qa1Y130_provenance
{
dgn-np:NP1074119.RAkiKWi8EDc3jgmUjOHnJ_ch-qL9Nn6hRE0EpaOW8Qa1Y130_assertion
dcterms:description
"[Mutations in MYO6 encoding an atypical myosin motor protein important for inner ear hair cell function have been associated with autosomal recessive (DFNB37) and autosomal dominant (DFNA22) types of hearing loss in a few families worldwide.]. 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:23635807
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1074119.RAkiKWi8EDc3jgmUjOHnJ_ch-qL9Nn6hRE0EpaOW8Qa1Y130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:53+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}