@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP550617.RAqLS6jONdVKZ4ShJaVu_pihR6glatapQTlsTqX3F5aRY
> .
@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:NP550617.RAqLS6jONdVKZ4ShJaVu_pihR6glatapQTlsTqX3F5aRY130_head
{
this:
np:hasAssertion
dgn-np:NP550617.RAqLS6jONdVKZ4ShJaVu_pihR6glatapQTlsTqX3F5aRY130_assertion
;
np:hasProvenance
dgn-np:NP550617.RAqLS6jONdVKZ4ShJaVu_pihR6glatapQTlsTqX3F5aRY130_provenance
;
np:hasPublicationInfo
dgn-np:NP550617.RAqLS6jONdVKZ4ShJaVu_pihR6glatapQTlsTqX3F5aRY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP550617.RAqLS6jONdVKZ4ShJaVu_pihR6glatapQTlsTqX3F5aRY130_assertion
a
np:Assertion
.
dgn-np:NP550617.RAqLS6jONdVKZ4ShJaVu_pihR6glatapQTlsTqX3F5aRY130_provenance
a
np:Provenance
.
dgn-np:NP550617.RAqLS6jONdVKZ4ShJaVu_pihR6glatapQTlsTqX3F5aRY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP550617.RAqLS6jONdVKZ4ShJaVu_pihR6glatapQTlsTqX3F5aRY130_assertion
{
miriam-gene:5827
a
ncit:C16612
.
lld:C0151313
a
ncit:C7057
.
dgn-gda:DGNc7ac38647281f9dac9a2838c7806a622
sio:SIO_000628
miriam-gene:5827
,
lld:C0151313
;
a
sio:SIO_001121
.
}
dgn-np:NP550617.RAqLS6jONdVKZ4ShJaVu_pihR6glatapQTlsTqX3F5aRY130_provenance
{
dgn-np:NP550617.RAqLS6jONdVKZ4ShJaVu_pihR6glatapQTlsTqX3F5aRY130_assertion
dcterms:description
"[Therefore, the relationship between the transverse axonal area and the number of myelin lamellae was morphometrically studied in myelinated fibers of the sural nerves in CMT 1A with PMP22 gene duplication to re-evaluate such relationships as are revealed in hereditary motor sensory neuropathy, type 1 without genetic diagnosis.]. 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:10862406
;
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:NP550617.RAqLS6jONdVKZ4ShJaVu_pihR6glatapQTlsTqX3F5aRY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:32+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" .
}