@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M
> .
@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:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_head
{
this:
np:hasAssertion
dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion
;
np:hasProvenance
dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance
;
np:hasPublicationInfo
dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion
a
np:Assertion
.
dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance
a
np:Provenance
.
dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C1846647
a
ncit:C7057
.
dgn-gda:DGN56a148a5968305ec370efeeca7ce93df
sio:SIO_000628
miriam-gene:2706
,
lld:C1846647
;
a
sio:SIO_001122
.
}
dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance
{
dgn-np:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion
dcterms:description
"[The Cx26 mutant W77R, which has been implicated in autosomal recessive deafness, also failed to form functional gap channels by itself but did not significantly interfere with the function of wildtype Cx26.]. 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:9856479
;
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:NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:26+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" .
}