@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP426230.RAOf2B3SbzBMGuERQMJjoG6fMI3E0KTiRnWH8BSH1oMmA
> .
@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/v3.0.0/void/
> .
dgn-np:NP426230.RAOf2B3SbzBMGuERQMJjoG6fMI3E0KTiRnWH8BSH1oMmA130_head
{
this:
np:hasAssertion
dgn-np:NP426230.RAOf2B3SbzBMGuERQMJjoG6fMI3E0KTiRnWH8BSH1oMmA130_assertion
;
np:hasProvenance
dgn-np:NP426230.RAOf2B3SbzBMGuERQMJjoG6fMI3E0KTiRnWH8BSH1oMmA130_provenance
;
np:hasPublicationInfo
dgn-np:NP426230.RAOf2B3SbzBMGuERQMJjoG6fMI3E0KTiRnWH8BSH1oMmA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP426230.RAOf2B3SbzBMGuERQMJjoG6fMI3E0KTiRnWH8BSH1oMmA130_assertion
a
np:Assertion
.
dgn-np:NP426230.RAOf2B3SbzBMGuERQMJjoG6fMI3E0KTiRnWH8BSH1oMmA130_provenance
a
np:Provenance
.
dgn-np:NP426230.RAOf2B3SbzBMGuERQMJjoG6fMI3E0KTiRnWH8BSH1oMmA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP426230.RAOf2B3SbzBMGuERQMJjoG6fMI3E0KTiRnWH8BSH1oMmA130_assertion
{
miriam-gene:2705
a
ncit:C16612
.
lld:C3825627
a
ncit:C7057
.
dgn-gda:DGN07db8b6041999b127315d64094326177
sio:SIO_000628
miriam-gene:2705
,
lld:C3825627
;
a
sio:SIO_001122
.
}
dgn-np:NP426230.RAOf2B3SbzBMGuERQMJjoG6fMI3E0KTiRnWH8BSH1oMmA130_provenance
{
dgn-np:NP426230.RAOf2B3SbzBMGuERQMJjoG6fMI3E0KTiRnWH8BSH1oMmA130_assertion
dcterms:description
"[Cx32 mutations may cause central nervous system dysfunction by reducing the number of functioning gap junctions between oligodendrocytes and astrocytes, making both cells more susceptible to abnormalities of intercellular exchange of ions and small molecules in situations of metabolic stress.]. 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:12325071
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP426230.RAOf2B3SbzBMGuERQMJjoG6fMI3E0KTiRnWH8BSH1oMmA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:48+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}