@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY
> .
@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:NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_head
{
this:
np:hasAssertion
dgn-np:NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_assertion
;
np:hasProvenance
dgn-np:NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_provenance
;
np:hasPublicationInfo
dgn-np:NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_assertion
a
np:Assertion
.
dgn-np:NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_provenance
a
np:Provenance
.
dgn-np:NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_assertion
{
miriam-gene:100128922
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGN8fef4800f5bfa001a33bd97b6244a3d8
sio:SIO_000628
miriam-gene:100128922
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_provenance
{
dgn-np:NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_assertion
dcterms:description
"[Interestingly, mutations of connexin genes have been reported in several human diseases (peripheral neuropathies, cardiovascular and dermatological diseases, hereditary cataract, and deafness) and altered expression of connexins have been associated with tumoral progression.]. 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:16677845
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}