@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP364738.RAKpSxRjEv7hPDvYAkeI96_7QmGu6fpAjWggtYYkyGHik
> .
@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:NP364738.RAKpSxRjEv7hPDvYAkeI96_7QmGu6fpAjWggtYYkyGHik130_head
{
this:
np:hasAssertion
dgn-np:NP364738.RAKpSxRjEv7hPDvYAkeI96_7QmGu6fpAjWggtYYkyGHik130_assertion
;
np:hasProvenance
dgn-np:NP364738.RAKpSxRjEv7hPDvYAkeI96_7QmGu6fpAjWggtYYkyGHik130_provenance
;
np:hasPublicationInfo
dgn-np:NP364738.RAKpSxRjEv7hPDvYAkeI96_7QmGu6fpAjWggtYYkyGHik130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP364738.RAKpSxRjEv7hPDvYAkeI96_7QmGu6fpAjWggtYYkyGHik130_assertion
a
np:Assertion
.
dgn-np:NP364738.RAKpSxRjEv7hPDvYAkeI96_7QmGu6fpAjWggtYYkyGHik130_provenance
a
np:Provenance
.
dgn-np:NP364738.RAKpSxRjEv7hPDvYAkeI96_7QmGu6fpAjWggtYYkyGHik130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP364738.RAKpSxRjEv7hPDvYAkeI96_7QmGu6fpAjWggtYYkyGHik130_assertion
{
miriam-gene:7466
a
ncit:C16612
.
lld:C0043207
a
ncit:C7057
.
dgn-gda:DGNf44018cfa5b542fa35e1695ec27e1e77
sio:SIO_000628
miriam-gene:7466
,
lld:C0043207
;
a
sio:SIO_001121
.
}
dgn-np:NP364738.RAKpSxRjEv7hPDvYAkeI96_7QmGu6fpAjWggtYYkyGHik130_provenance
{
dgn-np:NP364738.RAKpSxRjEv7hPDvYAkeI96_7QmGu6fpAjWggtYYkyGHik130_assertion
dcterms:description
"[An LFSNHL locus has recently been assigned to chromosome 4p16, and mutations in WFS1, the causative gene for Wolfram syndrome, have been found to cause LFSNHL in families with DFNA6, DFNA14, or DFNA38.]. 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:12181639
;
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:NP364738.RAKpSxRjEv7hPDvYAkeI96_7QmGu6fpAjWggtYYkyGHik130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:30+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" .
}