@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw
> .
@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:NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_head
{
this:
np:hasAssertion
dgn-np:NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_assertion
;
np:hasProvenance
dgn-np:NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_provenance
;
np:hasPublicationInfo
dgn-np:NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_assertion
a
np:Assertion
.
dgn-np:NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_provenance
a
np:Provenance
.
dgn-np:NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_assertion
{
miriam-gene:6683
a
ncit:C16612
.
lld:C0037773
a
ncit:C7057
.
dgn-gda:DGN528c127feaa54ac8eeac669c11839c45
sio:SIO_000628
miriam-gene:6683
,
lld:C0037773
;
a
sio:SIO_001122
.
}
dgn-np:NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_provenance
{
dgn-np:NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_assertion
dcterms:description
"[These results suggest that the frequency of SPAST mutations is higher among Japanese patients with autosomal dominant Hereditary spastic paraplegia (HSP), although SPAST mutations are also observed in patients with sporadic spastic paraplegia.]. 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:16788734
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP141620.RAwVPdaFn19gqP6_eTk1PR9brsqlikklL9qHoCNJA9Vaw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:14+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" .
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pav:version
"v2.1.0" .
}