@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_assertion
a
np:Assertion
.
dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_provenance
a
np:Provenance
.
dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_assertion
{
miriam-gene:23562
a
ncit:C16612
.
lld:C0581883
a
ncit:C7057
.
dgn-gda:DGNed1b2152d95c2df685c101478e33a4ad
sio:SIO_000628
miriam-gene:23562
,
lld:C0581883
;
a
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.
}
dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_provenance
{
dgn-np:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_assertion
dcterms:description
"[The essential function of one of these claudins in the inner ear was established by identifying mutations in CLDN14 that cause nonsyndromic recessive deafness DFNB29 in two large consanguineous Pakistani families.]. 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:11163249
;
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:NP913891.RAZJ3_Oul-uOMQPrJuoeEulgvs8YPgs96PYufPbQpVfmk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:20+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
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pav:authoredBy
<
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
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"v2.1.0" .
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