@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc
> .
@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/v4.0.0/void/
> .
dgn-np:NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_head
{
this:
np:hasAssertion
dgn-np:NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_assertion
;
np:hasProvenance
dgn-np:NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_provenance
;
np:hasPublicationInfo
dgn-np:NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_assertion
a
np:Assertion
.
dgn-np:NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_provenance
a
np:Provenance
.
dgn-np:NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C0018784
a
ncit:C7057
.
dgn-gda:DGNde5907c747ea21509a790242000af659
sio:SIO_000628
miriam-gene:2706
,
lld:C0018784
;
a
sio:SIO_001121
.
}
dgn-np:NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_provenance
{
dgn-np:NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_assertion
dcterms:description
"[Most probands have a congenital HL that is stable, symmetrical and without associated manifestations, but the audiometric profile should not be the only criteria for offering mutational screening of DFNB1 because of the observed variability.]. 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:18758381
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP690552.RACCDDkajB8M5IP2DC0B7jCwB6WKztvfB_KStDpbXTdfc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:58+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}