@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP159874.RAX-OZeqZLpmbmhM-8er8rMSw8gUBB9UuWjPT7-e1Ygpo
> .
@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:NP159874.RAX-OZeqZLpmbmhM-8er8rMSw8gUBB9UuWjPT7-e1Ygpo130_head
{
this:
np:hasAssertion
dgn-np:NP159874.RAX-OZeqZLpmbmhM-8er8rMSw8gUBB9UuWjPT7-e1Ygpo130_assertion
;
np:hasProvenance
dgn-np:NP159874.RAX-OZeqZLpmbmhM-8er8rMSw8gUBB9UuWjPT7-e1Ygpo130_provenance
;
np:hasPublicationInfo
dgn-np:NP159874.RAX-OZeqZLpmbmhM-8er8rMSw8gUBB9UuWjPT7-e1Ygpo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP159874.RAX-OZeqZLpmbmhM-8er8rMSw8gUBB9UuWjPT7-e1Ygpo130_assertion
a
np:Assertion
.
dgn-np:NP159874.RAX-OZeqZLpmbmhM-8er8rMSw8gUBB9UuWjPT7-e1Ygpo130_provenance
a
np:Provenance
.
dgn-np:NP159874.RAX-OZeqZLpmbmhM-8er8rMSw8gUBB9UuWjPT7-e1Ygpo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP159874.RAX-OZeqZLpmbmhM-8er8rMSw8gUBB9UuWjPT7-e1Ygpo130_assertion
{
miriam-gene:5172
a
ncit:C16612
.
lld:C0152268
a
ncit:C7057
.
dgn-gda:DGN2424eaeecde0393148b1aaeee11f1431
sio:SIO_000628
miriam-gene:5172
,
lld:C0152268
;
a
sio:SIO_001121
.
}
dgn-np:NP159874.RAX-OZeqZLpmbmhM-8er8rMSw8gUBB9UuWjPT7-e1Ygpo130_provenance
{
dgn-np:NP159874.RAX-OZeqZLpmbmhM-8er8rMSw8gUBB9UuWjPT7-e1Ygpo130_assertion
dcterms:description
"[GJB2 mutation was frequent in sporadic outpatients and its mutation frequency was significant higher in the prelingual group than in the postlingual group, whereas the mutation of mtDNA A1555G and SLC26A4 was very rare in Chinese sporadic outpatients with nonsyndromic sensorineural hearing loss (NSHL).]. 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:21162657
;
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:NP159874.RAX-OZeqZLpmbmhM-8er8rMSw8gUBB9UuWjPT7-e1Ygpo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+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" .
}