@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1097293.RApGbHaz_yNap-bpix8RBti0CDmTNiLOKIucQTEnFB2Fs
> .
@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:NP1097293.RApGbHaz_yNap-bpix8RBti0CDmTNiLOKIucQTEnFB2Fs130_head
{
this:
np:hasAssertion
dgn-np:NP1097293.RApGbHaz_yNap-bpix8RBti0CDmTNiLOKIucQTEnFB2Fs130_assertion
;
np:hasProvenance
dgn-np:NP1097293.RApGbHaz_yNap-bpix8RBti0CDmTNiLOKIucQTEnFB2Fs130_provenance
;
np:hasPublicationInfo
dgn-np:NP1097293.RApGbHaz_yNap-bpix8RBti0CDmTNiLOKIucQTEnFB2Fs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1097293.RApGbHaz_yNap-bpix8RBti0CDmTNiLOKIucQTEnFB2Fs130_assertion
a
np:Assertion
.
dgn-np:NP1097293.RApGbHaz_yNap-bpix8RBti0CDmTNiLOKIucQTEnFB2Fs130_provenance
a
np:Provenance
.
dgn-np:NP1097293.RApGbHaz_yNap-bpix8RBti0CDmTNiLOKIucQTEnFB2Fs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1097293.RApGbHaz_yNap-bpix8RBti0CDmTNiLOKIucQTEnFB2Fs130_assertion
{
miriam-gene:5376
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGNeb3ca41807b1aecc80d4d629ac212d1c
sio:SIO_000628
miriam-gene:5376
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP1097293.RApGbHaz_yNap-bpix8RBti0CDmTNiLOKIucQTEnFB2Fs130_provenance
{
dgn-np:NP1097293.RApGbHaz_yNap-bpix8RBti0CDmTNiLOKIucQTEnFB2Fs130_assertion
dcterms:description
"[The presence of concomitant diseases shows a tendency to worsen the clinical and neurophysiological CMT1A phenotype, especially in patients with CMT1A and diabetes mellitus, where higher values in the CMT neuropathy score and clinical motor subscore have been observed.]. 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:23891256
;
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:NP1097293.RApGbHaz_yNap-bpix8RBti0CDmTNiLOKIucQTEnFB2Fs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:03+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" .
}