@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP919805.RArbKB28vt54DJ0zPeK_PFRUfobmluaEoQC7NQXYlLquU
> .
@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:NP919805.RArbKB28vt54DJ0zPeK_PFRUfobmluaEoQC7NQXYlLquU130_head
{
this:
np:hasAssertion
dgn-np:NP919805.RArbKB28vt54DJ0zPeK_PFRUfobmluaEoQC7NQXYlLquU130_assertion
;
np:hasProvenance
dgn-np:NP919805.RArbKB28vt54DJ0zPeK_PFRUfobmluaEoQC7NQXYlLquU130_provenance
;
np:hasPublicationInfo
dgn-np:NP919805.RArbKB28vt54DJ0zPeK_PFRUfobmluaEoQC7NQXYlLquU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP919805.RArbKB28vt54DJ0zPeK_PFRUfobmluaEoQC7NQXYlLquU130_assertion
a
np:Assertion
.
dgn-np:NP919805.RArbKB28vt54DJ0zPeK_PFRUfobmluaEoQC7NQXYlLquU130_provenance
a
np:Provenance
.
dgn-np:NP919805.RArbKB28vt54DJ0zPeK_PFRUfobmluaEoQC7NQXYlLquU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP919805.RArbKB28vt54DJ0zPeK_PFRUfobmluaEoQC7NQXYlLquU130_assertion
{
miriam-gene:5376
a
ncit:C16612
.
lld:C0151313
a
ncit:C7057
.
dgn-gda:DGN1a086c1c46bf3174e668162e5aac1796
sio:SIO_000628
miriam-gene:5376
,
lld:C0151313
;
a
sio:SIO_001121
.
}
dgn-np:NP919805.RArbKB28vt54DJ0zPeK_PFRUfobmluaEoQC7NQXYlLquU130_provenance
{
dgn-np:NP919805.RArbKB28vt54DJ0zPeK_PFRUfobmluaEoQC7NQXYlLquU130_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:NP919805.RArbKB28vt54DJ0zPeK_PFRUfobmluaEoQC7NQXYlLquU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:24+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" .
}