@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP74431.RAMn8E4nZBuRo5CGwZ_hGjZ9HcVd6cKMmQGxW2iQj8rc0
> .
@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:NP74431.RAMn8E4nZBuRo5CGwZ_hGjZ9HcVd6cKMmQGxW2iQj8rc0130_head
{
this:
np:hasAssertion
dgn-np:NP74431.RAMn8E4nZBuRo5CGwZ_hGjZ9HcVd6cKMmQGxW2iQj8rc0130_assertion
;
np:hasProvenance
dgn-np:NP74431.RAMn8E4nZBuRo5CGwZ_hGjZ9HcVd6cKMmQGxW2iQj8rc0130_provenance
;
np:hasPublicationInfo
dgn-np:NP74431.RAMn8E4nZBuRo5CGwZ_hGjZ9HcVd6cKMmQGxW2iQj8rc0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP74431.RAMn8E4nZBuRo5CGwZ_hGjZ9HcVd6cKMmQGxW2iQj8rc0130_assertion
a
np:Assertion
.
dgn-np:NP74431.RAMn8E4nZBuRo5CGwZ_hGjZ9HcVd6cKMmQGxW2iQj8rc0130_provenance
a
np:Provenance
.
dgn-np:NP74431.RAMn8E4nZBuRo5CGwZ_hGjZ9HcVd6cKMmQGxW2iQj8rc0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP74431.RAMn8E4nZBuRo5CGwZ_hGjZ9HcVd6cKMmQGxW2iQj8rc0130_assertion
{
miriam-gene:10804
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGN0d3c10bd79d8b1364bef88107f060026
sio:SIO_000628
miriam-gene:10804
,
lld:C0011053
;
a
sio:SIO_001122
.
}
dgn-np:NP74431.RAMn8E4nZBuRo5CGwZ_hGjZ9HcVd6cKMmQGxW2iQj8rc0130_provenance
{
dgn-np:NP74431.RAMn8E4nZBuRo5CGwZ_hGjZ9HcVd6cKMmQGxW2iQj8rc0130_assertion
dcterms:description
"[Aiming at establishing the frequencies of GJB2 mutations and GJB6 deletions in the Brazilian population, we screened 300 unrelated individuals with hearing impairment, who were not affected by known deafness related syndromes.]. 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:19125024
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP74431.RAMn8E4nZBuRo5CGwZ_hGjZ9HcVd6cKMmQGxW2iQj8rc0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:36+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" .
}