@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP370784.RAhoeBIx6XIQtWexC-05IO1i_Cm_b5CEV-YOwzFq5Hqu0
> .
@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:NP370784.RAhoeBIx6XIQtWexC-05IO1i_Cm_b5CEV-YOwzFq5Hqu0130_head
{
this:
np:hasAssertion
dgn-np:NP370784.RAhoeBIx6XIQtWexC-05IO1i_Cm_b5CEV-YOwzFq5Hqu0130_assertion
;
np:hasProvenance
dgn-np:NP370784.RAhoeBIx6XIQtWexC-05IO1i_Cm_b5CEV-YOwzFq5Hqu0130_provenance
;
np:hasPublicationInfo
dgn-np:NP370784.RAhoeBIx6XIQtWexC-05IO1i_Cm_b5CEV-YOwzFq5Hqu0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP370784.RAhoeBIx6XIQtWexC-05IO1i_Cm_b5CEV-YOwzFq5Hqu0130_assertion
a
np:Assertion
.
dgn-np:NP370784.RAhoeBIx6XIQtWexC-05IO1i_Cm_b5CEV-YOwzFq5Hqu0130_provenance
a
np:Provenance
.
dgn-np:NP370784.RAhoeBIx6XIQtWexC-05IO1i_Cm_b5CEV-YOwzFq5Hqu0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP370784.RAhoeBIx6XIQtWexC-05IO1i_Cm_b5CEV-YOwzFq5Hqu0130_assertion
{
miriam-gene:9381
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGN5960358ed3583c3a1292fed57689503c
sio:SIO_000628
miriam-gene:9381
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP370784.RAhoeBIx6XIQtWexC-05IO1i_Cm_b5CEV-YOwzFq5Hqu0130_provenance
{
dgn-np:NP370784.RAhoeBIx6XIQtWexC-05IO1i_Cm_b5CEV-YOwzFq5Hqu0130_assertion
dcterms:description
"[Mutations of four common deafness-associated genes, GJB2, SLC26A4, the mitochondrial 12S rRNA gene, and OTOF, were screened in 743 unrelated children with idiopathic sensorineural hearing impairment, including 180 and 563 children with and without CIs, respectively.]. 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:21557232
;
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:NP370784.RAhoeBIx6XIQtWexC-05IO1i_Cm_b5CEV-YOwzFq5Hqu0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:37+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" .
}