@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP685819.RANkaV3squpgdMNlSVTRb6FY95a8kdT6GxGAsBVEmlIM0
> .
@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:NP685819.RANkaV3squpgdMNlSVTRb6FY95a8kdT6GxGAsBVEmlIM0130_head
{
this:
np:hasAssertion
dgn-np:NP685819.RANkaV3squpgdMNlSVTRb6FY95a8kdT6GxGAsBVEmlIM0130_assertion
;
np:hasProvenance
dgn-np:NP685819.RANkaV3squpgdMNlSVTRb6FY95a8kdT6GxGAsBVEmlIM0130_provenance
;
np:hasPublicationInfo
dgn-np:NP685819.RANkaV3squpgdMNlSVTRb6FY95a8kdT6GxGAsBVEmlIM0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP685819.RANkaV3squpgdMNlSVTRb6FY95a8kdT6GxGAsBVEmlIM0130_assertion
a
np:Assertion
.
dgn-np:NP685819.RANkaV3squpgdMNlSVTRb6FY95a8kdT6GxGAsBVEmlIM0130_provenance
a
np:Provenance
.
dgn-np:NP685819.RANkaV3squpgdMNlSVTRb6FY95a8kdT6GxGAsBVEmlIM0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP685819.RANkaV3squpgdMNlSVTRb6FY95a8kdT6GxGAsBVEmlIM0130_assertion
{
miriam-gene:4359
a
ncit:C16612
.
lld:C0393819
a
ncit:C7057
.
dgn-gda:DGN94a3badc4041127cc6df298bb70c02c6
sio:SIO_000628
miriam-gene:4359
,
lld:C0393819
;
a
sio:SIO_001121
.
}
dgn-np:NP685819.RANkaV3squpgdMNlSVTRb6FY95a8kdT6GxGAsBVEmlIM0130_provenance
{
dgn-np:NP685819.RANkaV3squpgdMNlSVTRb6FY95a8kdT6GxGAsBVEmlIM0130_assertion
dcterms:description
"[The average fold change of the 5 genes over normal expression, as determined by qPCR, was significantly elevated in skin biopsies from patients with CIDP in comparison to CMT1 or diabetic neuropathy, and similar to that seen in Lyme disease.]. 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:19922956
;
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:NP685819.RANkaV3squpgdMNlSVTRb6FY95a8kdT6GxGAsBVEmlIM0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:57+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" .
}