@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP414883.RANjUXCFczYTKl8N0sv78WiRZpiCHNiFDy-11q_gDzpV0
> .
@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:NP414883.RANjUXCFczYTKl8N0sv78WiRZpiCHNiFDy-11q_gDzpV0130_head
{
this:
np:hasAssertion
dgn-np:NP414883.RANjUXCFczYTKl8N0sv78WiRZpiCHNiFDy-11q_gDzpV0130_assertion
;
np:hasProvenance
dgn-np:NP414883.RANjUXCFczYTKl8N0sv78WiRZpiCHNiFDy-11q_gDzpV0130_provenance
;
np:hasPublicationInfo
dgn-np:NP414883.RANjUXCFczYTKl8N0sv78WiRZpiCHNiFDy-11q_gDzpV0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP414883.RANjUXCFczYTKl8N0sv78WiRZpiCHNiFDy-11q_gDzpV0130_assertion
a
np:Assertion
.
dgn-np:NP414883.RANjUXCFczYTKl8N0sv78WiRZpiCHNiFDy-11q_gDzpV0130_provenance
a
np:Provenance
.
dgn-np:NP414883.RANjUXCFczYTKl8N0sv78WiRZpiCHNiFDy-11q_gDzpV0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP414883.RANjUXCFczYTKl8N0sv78WiRZpiCHNiFDy-11q_gDzpV0130_assertion
{
miriam-gene:10989
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGNa7b7d5d16c43fb9c13c326cb9511966f
sio:SIO_000628
miriam-gene:10989
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP414883.RANjUXCFczYTKl8N0sv78WiRZpiCHNiFDy-11q_gDzpV0130_provenance
{
dgn-np:NP414883.RANjUXCFczYTKl8N0sv78WiRZpiCHNiFDy-11q_gDzpV0130_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-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:NP414883.RANjUXCFczYTKl8N0sv78WiRZpiCHNiFDy-11q_gDzpV0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:06+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" .
}