@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP387734.RAAuXGWxabAbFU_L41iBbwYyOxWlnCLx9QfNA6qbQegT0
> .
@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:NP387734.RAAuXGWxabAbFU_L41iBbwYyOxWlnCLx9QfNA6qbQegT0130_head
{
this:
np:hasAssertion
dgn-np:NP387734.RAAuXGWxabAbFU_L41iBbwYyOxWlnCLx9QfNA6qbQegT0130_assertion
;
np:hasProvenance
dgn-np:NP387734.RAAuXGWxabAbFU_L41iBbwYyOxWlnCLx9QfNA6qbQegT0130_provenance
;
np:hasPublicationInfo
dgn-np:NP387734.RAAuXGWxabAbFU_L41iBbwYyOxWlnCLx9QfNA6qbQegT0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP387734.RAAuXGWxabAbFU_L41iBbwYyOxWlnCLx9QfNA6qbQegT0130_assertion
a
np:Assertion
.
dgn-np:NP387734.RAAuXGWxabAbFU_L41iBbwYyOxWlnCLx9QfNA6qbQegT0130_provenance
a
np:Provenance
.
dgn-np:NP387734.RAAuXGWxabAbFU_L41iBbwYyOxWlnCLx9QfNA6qbQegT0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP387734.RAAuXGWxabAbFU_L41iBbwYyOxWlnCLx9QfNA6qbQegT0130_assertion
{
miriam-gene:9897
a
ncit:C16612
.
lld:C0751602
a
ncit:C7057
.
dgn-gda:DGN33a7e394e3bf4a358e598335cc189910
sio:SIO_000628
miriam-gene:9897
,
lld:C0751602
;
a
sio:SIO_001121
.
}
dgn-np:NP387734.RAAuXGWxabAbFU_L41iBbwYyOxWlnCLx9QfNA6qbQegT0130_provenance
{
dgn-np:NP387734.RAAuXGWxabAbFU_L41iBbwYyOxWlnCLx9QfNA6qbQegT0130_assertion
dcterms:description
"[In this study, we compared spinal cord magnetic resonance imaging (MRI) in 13 HSP patients with four different types of autosomal dominant hereditary spastic paraplegia (SPG3A, SPG4, SPG6, and SPG8) with age-matched control subjects.]. 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:16143870
;
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:NP387734.RAAuXGWxabAbFU_L41iBbwYyOxWlnCLx9QfNA6qbQegT0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:51+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" .
}