@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1258799.RA_e_nC6i0cgmvFbTqMjVg_WxnlQS5Gwx1-gFUUXiOLTE
> .
@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:NP1258799.RA_e_nC6i0cgmvFbTqMjVg_WxnlQS5Gwx1-gFUUXiOLTE130_head
{
this:
np:hasAssertion
dgn-np:NP1258799.RA_e_nC6i0cgmvFbTqMjVg_WxnlQS5Gwx1-gFUUXiOLTE130_assertion
;
np:hasProvenance
dgn-np:NP1258799.RA_e_nC6i0cgmvFbTqMjVg_WxnlQS5Gwx1-gFUUXiOLTE130_provenance
;
np:hasPublicationInfo
dgn-np:NP1258799.RA_e_nC6i0cgmvFbTqMjVg_WxnlQS5Gwx1-gFUUXiOLTE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1258799.RA_e_nC6i0cgmvFbTqMjVg_WxnlQS5Gwx1-gFUUXiOLTE130_assertion
a
np:Assertion
.
dgn-np:NP1258799.RA_e_nC6i0cgmvFbTqMjVg_WxnlQS5Gwx1-gFUUXiOLTE130_provenance
a
np:Provenance
.
dgn-np:NP1258799.RA_e_nC6i0cgmvFbTqMjVg_WxnlQS5Gwx1-gFUUXiOLTE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1258799.RA_e_nC6i0cgmvFbTqMjVg_WxnlQS5Gwx1-gFUUXiOLTE130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C0265336
a
ncit:C7057
.
dgn-gda:DGNc6e64b8318abef08a09175f72d73e194
sio:SIO_000628
miriam-gene:2706
,
lld:C0265336
;
a
sio:SIO_001121
.
}
dgn-np:NP1258799.RA_e_nC6i0cgmvFbTqMjVg_WxnlQS5Gwx1-gFUUXiOLTE130_provenance
{
dgn-np:NP1258799.RA_e_nC6i0cgmvFbTqMjVg_WxnlQS5Gwx1-gFUUXiOLTE130_assertion
dcterms:description
"[Because in the human skin connexin 26 (Cx26) is co-expressed with other connexins, like Cx43 and Cx30, and as the KID syndrome is inherited as autosomal dominant condition, it is possible that KID mutations change the way Cx26 interacts with other co-expressed connexins.]. 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:25625422
;
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:NP1258799.RA_e_nC6i0cgmvFbTqMjVg_WxnlQS5Gwx1-gFUUXiOLTE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:17+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" .
}