@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP791743.RAQAZJRuXcFq8fOJ6GZYI1IgQmnlKVNCT1pUDXwA29KAk
> .
@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:NP791743.RAQAZJRuXcFq8fOJ6GZYI1IgQmnlKVNCT1pUDXwA29KAk130_head
{
this:
np:hasAssertion
dgn-np:NP791743.RAQAZJRuXcFq8fOJ6GZYI1IgQmnlKVNCT1pUDXwA29KAk130_assertion
;
np:hasProvenance
dgn-np:NP791743.RAQAZJRuXcFq8fOJ6GZYI1IgQmnlKVNCT1pUDXwA29KAk130_provenance
;
np:hasPublicationInfo
dgn-np:NP791743.RAQAZJRuXcFq8fOJ6GZYI1IgQmnlKVNCT1pUDXwA29KAk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP791743.RAQAZJRuXcFq8fOJ6GZYI1IgQmnlKVNCT1pUDXwA29KAk130_assertion
a
np:Assertion
.
dgn-np:NP791743.RAQAZJRuXcFq8fOJ6GZYI1IgQmnlKVNCT1pUDXwA29KAk130_provenance
a
np:Provenance
.
dgn-np:NP791743.RAQAZJRuXcFq8fOJ6GZYI1IgQmnlKVNCT1pUDXwA29KAk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP791743.RAQAZJRuXcFq8fOJ6GZYI1IgQmnlKVNCT1pUDXwA29KAk130_assertion
{
miriam-gene:2697
a
ncit:C16612
.
lld:C0155552
a
ncit:C7057
.
dgn-gda:DGNdb91bdc4a2da5a9012217a60d975be93
sio:SIO_000628
miriam-gene:2697
,
lld:C0155552
;
a
sio:SIO_001121
.
}
dgn-np:NP791743.RAQAZJRuXcFq8fOJ6GZYI1IgQmnlKVNCT1pUDXwA29KAk130_provenance
{
dgn-np:NP791743.RAQAZJRuXcFq8fOJ6GZYI1IgQmnlKVNCT1pUDXwA29KAk130_assertion
dcterms:description
"[The results of this study suggest that the three mutations in GJA1 or rhoGJA1 that we previously reported result in at least partial loss of normal functions carried out by CX43, which may form a basis for the mechanism contributing to hearing loss in patients.]. 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:20130915
;
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:NP791743.RAQAZJRuXcFq8fOJ6GZYI1IgQmnlKVNCT1pUDXwA29KAk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:44+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" .
}