@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP169467.RAwq4Eom2HN4G1ZUiUVxXeAyWO9lXFxYjPTXJRBb8WG9w
> .
@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:NP169467.RAwq4Eom2HN4G1ZUiUVxXeAyWO9lXFxYjPTXJRBb8WG9w130_head
{
this:
np:hasAssertion
dgn-np:NP169467.RAwq4Eom2HN4G1ZUiUVxXeAyWO9lXFxYjPTXJRBb8WG9w130_assertion
;
np:hasProvenance
dgn-np:NP169467.RAwq4Eom2HN4G1ZUiUVxXeAyWO9lXFxYjPTXJRBb8WG9w130_provenance
;
np:hasPublicationInfo
dgn-np:NP169467.RAwq4Eom2HN4G1ZUiUVxXeAyWO9lXFxYjPTXJRBb8WG9w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP169467.RAwq4Eom2HN4G1ZUiUVxXeAyWO9lXFxYjPTXJRBb8WG9w130_assertion
a
np:Assertion
.
dgn-np:NP169467.RAwq4Eom2HN4G1ZUiUVxXeAyWO9lXFxYjPTXJRBb8WG9w130_provenance
a
np:Provenance
.
dgn-np:NP169467.RAwq4Eom2HN4G1ZUiUVxXeAyWO9lXFxYjPTXJRBb8WG9w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP169467.RAwq4Eom2HN4G1ZUiUVxXeAyWO9lXFxYjPTXJRBb8WG9w130_assertion
{
miriam-gene:51168
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGN05120e1bdaeb492e7b11f70c871db7c0
sio:SIO_000628
miriam-gene:51168
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP169467.RAwq4Eom2HN4G1ZUiUVxXeAyWO9lXFxYjPTXJRBb8WG9w130_provenance
{
dgn-np:NP169467.RAwq4Eom2HN4G1ZUiUVxXeAyWO9lXFxYjPTXJRBb8WG9w130_assertion
dcterms:description
"[Given the extensive consanguinity of the pedigree, there might be at least one more deafness locus segregating to explain the condition in some of the subjects whose deafness is not clearly associated with MYO15A mutations, although overlooked environmental causes could not be ruled out.]. 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:17851452
;
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:NP169467.RAwq4Eom2HN4G1ZUiUVxXeAyWO9lXFxYjPTXJRBb8WG9w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+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" .
}