@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP426078.RAjkmVsR12UKeSiz2PBYAI7iYympopHVk6ihrOmn9bZRQ
> .
@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:NP426078.RAjkmVsR12UKeSiz2PBYAI7iYympopHVk6ihrOmn9bZRQ130_head
{
this:
np:hasAssertion
dgn-np:NP426078.RAjkmVsR12UKeSiz2PBYAI7iYympopHVk6ihrOmn9bZRQ130_assertion
;
np:hasProvenance
dgn-np:NP426078.RAjkmVsR12UKeSiz2PBYAI7iYympopHVk6ihrOmn9bZRQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP426078.RAjkmVsR12UKeSiz2PBYAI7iYympopHVk6ihrOmn9bZRQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP426078.RAjkmVsR12UKeSiz2PBYAI7iYympopHVk6ihrOmn9bZRQ130_assertion
a
np:Assertion
.
dgn-np:NP426078.RAjkmVsR12UKeSiz2PBYAI7iYympopHVk6ihrOmn9bZRQ130_provenance
a
np:Provenance
.
dgn-np:NP426078.RAjkmVsR12UKeSiz2PBYAI7iYympopHVk6ihrOmn9bZRQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP426078.RAjkmVsR12UKeSiz2PBYAI7iYympopHVk6ihrOmn9bZRQ130_assertion
{
miriam-gene:2705
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN1a952dad2b01a34c5593c7ffd28934d2
sio:SIO_000628
miriam-gene:2705
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP426078.RAjkmVsR12UKeSiz2PBYAI7iYympopHVk6ihrOmn9bZRQ130_provenance
{
dgn-np:NP426078.RAjkmVsR12UKeSiz2PBYAI7iYympopHVk6ihrOmn9bZRQ130_assertion
dcterms:description
"[Because increasing cortical abnormalities correlate with disease progression and cognitive dysfunction, we examined the expression of oligodendrocytic connexin32 (Cx32) and Cx47 and their astrocytic partners Cx30 and Cx43 in cortical lesions and normal-appearing gray matter (NAGM) in MS patients.]. 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:25101702
;
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:NP426078.RAjkmVsR12UKeSiz2PBYAI7iYympopHVk6ihrOmn9bZRQ130_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" .
}