@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP644355.RA1btr7qJw-yvW3MXRIYJID9wkpbN4mkoAqMNL06mXs3Y
> .
@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:NP644355.RA1btr7qJw-yvW3MXRIYJID9wkpbN4mkoAqMNL06mXs3Y130_head
{
this:
np:hasAssertion
dgn-np:NP644355.RA1btr7qJw-yvW3MXRIYJID9wkpbN4mkoAqMNL06mXs3Y130_assertion
;
np:hasProvenance
dgn-np:NP644355.RA1btr7qJw-yvW3MXRIYJID9wkpbN4mkoAqMNL06mXs3Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP644355.RA1btr7qJw-yvW3MXRIYJID9wkpbN4mkoAqMNL06mXs3Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP644355.RA1btr7qJw-yvW3MXRIYJID9wkpbN4mkoAqMNL06mXs3Y130_assertion
a
np:Assertion
.
dgn-np:NP644355.RA1btr7qJw-yvW3MXRIYJID9wkpbN4mkoAqMNL06mXs3Y130_provenance
a
np:Provenance
.
dgn-np:NP644355.RA1btr7qJw-yvW3MXRIYJID9wkpbN4mkoAqMNL06mXs3Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP644355.RA1btr7qJw-yvW3MXRIYJID9wkpbN4mkoAqMNL06mXs3Y130_assertion
{
miriam-gene:2705
a
ncit:C16612
.
lld:C0026846
a
ncit:C7057
.
dgn-gda:DGNe3a94b9b8749442b95ce6aee8ec7dc29
sio:SIO_000628
miriam-gene:2705
,
lld:C0026846
;
a
sio:SIO_001121
.
}
dgn-np:NP644355.RA1btr7qJw-yvW3MXRIYJID9wkpbN4mkoAqMNL06mXs3Y130_provenance
{
dgn-np:NP644355.RA1btr7qJw-yvW3MXRIYJID9wkpbN4mkoAqMNL06mXs3Y130_assertion
dcterms:description
"[Axonal features of diminished amplitudes of compound muscle action potentials (CMAPs), axonal loss, axonal sprouting and neuropathic muscle wasting all changed as disease advanced, especially in PMP22 duplication and Cx32 mutations.]. 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:12477701
;
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:NP644355.RA1btr7qJw-yvW3MXRIYJID9wkpbN4mkoAqMNL06mXs3Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:28+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" .
}