@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP727293.RAd01C2R0jG_B_afaa5ZPXI3K7cCKdqVlvS7QZKl4qY5o
> .
@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/v3.0.0/void/
> .
dgn-np:NP727293.RAd01C2R0jG_B_afaa5ZPXI3K7cCKdqVlvS7QZKl4qY5o130_head
{
this:
np:hasAssertion
dgn-np:NP727293.RAd01C2R0jG_B_afaa5ZPXI3K7cCKdqVlvS7QZKl4qY5o130_assertion
;
np:hasProvenance
dgn-np:NP727293.RAd01C2R0jG_B_afaa5ZPXI3K7cCKdqVlvS7QZKl4qY5o130_provenance
;
np:hasPublicationInfo
dgn-np:NP727293.RAd01C2R0jG_B_afaa5ZPXI3K7cCKdqVlvS7QZKl4qY5o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP727293.RAd01C2R0jG_B_afaa5ZPXI3K7cCKdqVlvS7QZKl4qY5o130_assertion
a
np:Assertion
.
dgn-np:NP727293.RAd01C2R0jG_B_afaa5ZPXI3K7cCKdqVlvS7QZKl4qY5o130_provenance
a
np:Provenance
.
dgn-np:NP727293.RAd01C2R0jG_B_afaa5ZPXI3K7cCKdqVlvS7QZKl4qY5o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP727293.RAd01C2R0jG_B_afaa5ZPXI3K7cCKdqVlvS7QZKl4qY5o130_assertion
{
miriam-gene:7007
a
ncit:C16612
.
lld:C0018784
a
ncit:C7057
.
dgn-gda:DGN2034cede29de8881235b38829fd57c4d
sio:SIO_000628
miriam-gene:7007
,
lld:C0018784
;
a
sio:SIO_001121
.
}
dgn-np:NP727293.RAd01C2R0jG_B_afaa5ZPXI3K7cCKdqVlvS7QZKl4qY5o130_provenance
{
dgn-np:NP727293.RAd01C2R0jG_B_afaa5ZPXI3K7cCKdqVlvS7QZKl4qY5o130_assertion
dcterms:description
"[Although clinical data and genetic analysis for TECTA gene have been reported from different groups, there is no report that compound heterozygous mutations in the TECTA gene result in nonsyndromic sensorineural 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:22037481
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP727293.RAd01C2R0jG_B_afaa5ZPXI3K7cCKdqVlvS7QZKl4qY5o130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:58+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}