@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1356219.RAW_APbNmGAdepe_yx6_-je3dzvoGeE7_QFAepIGfZ9yc
> .
@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:NP1356219.RAW_APbNmGAdepe_yx6_-je3dzvoGeE7_QFAepIGfZ9yc130_head
{
this:
np:hasAssertion
dgn-np:NP1356219.RAW_APbNmGAdepe_yx6_-je3dzvoGeE7_QFAepIGfZ9yc130_assertion
;
np:hasProvenance
dgn-np:NP1356219.RAW_APbNmGAdepe_yx6_-je3dzvoGeE7_QFAepIGfZ9yc130_provenance
;
np:hasPublicationInfo
dgn-np:NP1356219.RAW_APbNmGAdepe_yx6_-je3dzvoGeE7_QFAepIGfZ9yc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1356219.RAW_APbNmGAdepe_yx6_-je3dzvoGeE7_QFAepIGfZ9yc130_assertion
a
np:Assertion
.
dgn-np:NP1356219.RAW_APbNmGAdepe_yx6_-je3dzvoGeE7_QFAepIGfZ9yc130_provenance
a
np:Provenance
.
dgn-np:NP1356219.RAW_APbNmGAdepe_yx6_-je3dzvoGeE7_QFAepIGfZ9yc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1356219.RAW_APbNmGAdepe_yx6_-je3dzvoGeE7_QFAepIGfZ9yc130_assertion
{
miriam-gene:4647
a
ncit:C16612
.
lld:C0155552
a
ncit:C7057
.
dgn-gda:DGN4b6747653b0aad0050dfe9873b3112c5
sio:SIO_000628
miriam-gene:4647
,
lld:C0155552
;
a
sio:SIO_001121
.
}
dgn-np:NP1356219.RAW_APbNmGAdepe_yx6_-je3dzvoGeE7_QFAepIGfZ9yc130_provenance
{
dgn-np:NP1356219.RAW_APbNmGAdepe_yx6_-je3dzvoGeE7_QFAepIGfZ9yc130_assertion
dcterms:description
"[Since it has been reported that another gene for dominant non-syndromic hearing loss (DFNA3) has been mapped to the same region as the first gene for recessive hearing loss (DFNB1), it is possible that different mutations in the DFNB2 gene may result in either dominant or recessive hearing loss.]. 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:8776602
;
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:NP1356219.RAW_APbNmGAdepe_yx6_-je3dzvoGeE7_QFAepIGfZ9yc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:01+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" .
}