@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP436246.RAUhMa2ZOmJP9-y7bwUWW7E_SuB9wU_m1APeXm-fuqbD0
> .
@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:NP436246.RAUhMa2ZOmJP9-y7bwUWW7E_SuB9wU_m1APeXm-fuqbD0130_head
{
this:
np:hasAssertion
dgn-np:NP436246.RAUhMa2ZOmJP9-y7bwUWW7E_SuB9wU_m1APeXm-fuqbD0130_assertion
;
np:hasProvenance
dgn-np:NP436246.RAUhMa2ZOmJP9-y7bwUWW7E_SuB9wU_m1APeXm-fuqbD0130_provenance
;
np:hasPublicationInfo
dgn-np:NP436246.RAUhMa2ZOmJP9-y7bwUWW7E_SuB9wU_m1APeXm-fuqbD0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP436246.RAUhMa2ZOmJP9-y7bwUWW7E_SuB9wU_m1APeXm-fuqbD0130_assertion
a
np:Assertion
.
dgn-np:NP436246.RAUhMa2ZOmJP9-y7bwUWW7E_SuB9wU_m1APeXm-fuqbD0130_provenance
a
np:Provenance
.
dgn-np:NP436246.RAUhMa2ZOmJP9-y7bwUWW7E_SuB9wU_m1APeXm-fuqbD0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP436246.RAUhMa2ZOmJP9-y7bwUWW7E_SuB9wU_m1APeXm-fuqbD0130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C0152268
a
ncit:C7057
.
dgn-gda:DGNbf3d59a8a4a392153cd843c9baaa06ad
sio:SIO_000628
miriam-gene:2706
,
lld:C0152268
;
a
sio:SIO_001121
.
}
dgn-np:NP436246.RAUhMa2ZOmJP9-y7bwUWW7E_SuB9wU_m1APeXm-fuqbD0130_provenance
{
dgn-np:NP436246.RAUhMa2ZOmJP9-y7bwUWW7E_SuB9wU_m1APeXm-fuqbD0130_assertion
dcterms:description
"[This study aimed to examine the mutations of the three common deafness genes GJB2, SLC26A4, and mtDNA A1555G in Chinese sporadic outpatients with NSHL and to discuss the factors that influence the detection accuracy of mutation frequencies.]. 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:NP436246.RAUhMa2ZOmJP9-y7bwUWW7E_SuB9wU_m1APeXm-fuqbD0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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" .
}