@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP426144.RARGlUKNByYZL82mLynAIArgit__Sy52_LrY3b7yM265o
> .
@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:NP426144.RARGlUKNByYZL82mLynAIArgit__Sy52_LrY3b7yM265o130_head
{
this:
np:hasAssertion
dgn-np:NP426144.RARGlUKNByYZL82mLynAIArgit__Sy52_LrY3b7yM265o130_assertion
;
np:hasProvenance
dgn-np:NP426144.RARGlUKNByYZL82mLynAIArgit__Sy52_LrY3b7yM265o130_provenance
;
np:hasPublicationInfo
dgn-np:NP426144.RARGlUKNByYZL82mLynAIArgit__Sy52_LrY3b7yM265o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP426144.RARGlUKNByYZL82mLynAIArgit__Sy52_LrY3b7yM265o130_assertion
a
np:Assertion
.
dgn-np:NP426144.RARGlUKNByYZL82mLynAIArgit__Sy52_LrY3b7yM265o130_provenance
a
np:Provenance
.
dgn-np:NP426144.RARGlUKNByYZL82mLynAIArgit__Sy52_LrY3b7yM265o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP426144.RARGlUKNByYZL82mLynAIArgit__Sy52_LrY3b7yM265o130_assertion
{
miriam-gene:2705
a
ncit:C16612
.
lld:C0393808
a
ncit:C7057
.
dgn-gda:DGN3af5d1057fc3c4e2a48ab1044f15bde0
sio:SIO_000628
miriam-gene:2705
,
lld:C0393808
;
a
sio:SIO_001121
.
}
dgn-np:NP426144.RARGlUKNByYZL82mLynAIArgit__Sy52_LrY3b7yM265o130_provenance
{
dgn-np:NP426144.RARGlUKNByYZL82mLynAIArgit__Sy52_LrY3b7yM265o130_assertion
dcterms:description
"[However, further studies are required to elucidate the exact mechanism by which CMTX mutant Cx32 proteins, which retain the ability to form homotypic junctional channels, damage Schwann cells and cause demyelinating neuropathy.]. 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:15006706
;
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:NP426144.RARGlUKNByYZL82mLynAIArgit__Sy52_LrY3b7yM265o130_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" .
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pav:version
"v3.0.0" .
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