@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP598507.RAVnCria_hK5CW7oUyhkFrgNyQ5pUD4uFx1XOfDkWaXZk
> .
@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:NP598507.RAVnCria_hK5CW7oUyhkFrgNyQ5pUD4uFx1XOfDkWaXZk130_head
{
this:
np:hasAssertion
dgn-np:NP598507.RAVnCria_hK5CW7oUyhkFrgNyQ5pUD4uFx1XOfDkWaXZk130_assertion
;
np:hasProvenance
dgn-np:NP598507.RAVnCria_hK5CW7oUyhkFrgNyQ5pUD4uFx1XOfDkWaXZk130_provenance
;
np:hasPublicationInfo
dgn-np:NP598507.RAVnCria_hK5CW7oUyhkFrgNyQ5pUD4uFx1XOfDkWaXZk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP598507.RAVnCria_hK5CW7oUyhkFrgNyQ5pUD4uFx1XOfDkWaXZk130_assertion
a
np:Assertion
.
dgn-np:NP598507.RAVnCria_hK5CW7oUyhkFrgNyQ5pUD4uFx1XOfDkWaXZk130_provenance
a
np:Provenance
.
dgn-np:NP598507.RAVnCria_hK5CW7oUyhkFrgNyQ5pUD4uFx1XOfDkWaXZk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP598507.RAVnCria_hK5CW7oUyhkFrgNyQ5pUD4uFx1XOfDkWaXZk130_assertion
{
miriam-gene:5827
a
ncit:C16612
.
lld:C0026846
a
ncit:C7057
.
dgn-gda:DGN8348b14fa32a9d2b3b01da542af009f8
sio:SIO_000628
miriam-gene:5827
,
lld:C0026846
;
a
sio:SIO_001121
.
}
dgn-np:NP598507.RAVnCria_hK5CW7oUyhkFrgNyQ5pUD4uFx1XOfDkWaXZk130_provenance
{
dgn-np:NP598507.RAVnCria_hK5CW7oUyhkFrgNyQ5pUD4uFx1XOfDkWaXZk130_assertion
dcterms:description
"[Transgenic models with extra copies of the Pmp22 gene have provided formal proof that overexpression of only this candidate gene is sufficent to cause peripheral demyelination, onion bulb formation, secondary axonal loss, and progressive muscle atrophy, the pathological hallmarks of CMT1A.]. 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:16775377
;
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:NP598507.RAVnCria_hK5CW7oUyhkFrgNyQ5pUD4uFx1XOfDkWaXZk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:59+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" .
}