@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP874721.RAf85nkajhcq5Va4MCtCZcU7ptpsK8EO97hShKIHlRIZA
> .
@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:NP874721.RAf85nkajhcq5Va4MCtCZcU7ptpsK8EO97hShKIHlRIZA130_head
{
this:
np:hasAssertion
dgn-np:NP874721.RAf85nkajhcq5Va4MCtCZcU7ptpsK8EO97hShKIHlRIZA130_assertion
;
np:hasProvenance
dgn-np:NP874721.RAf85nkajhcq5Va4MCtCZcU7ptpsK8EO97hShKIHlRIZA130_provenance
;
np:hasPublicationInfo
dgn-np:NP874721.RAf85nkajhcq5Va4MCtCZcU7ptpsK8EO97hShKIHlRIZA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP874721.RAf85nkajhcq5Va4MCtCZcU7ptpsK8EO97hShKIHlRIZA130_assertion
a
np:Assertion
.
dgn-np:NP874721.RAf85nkajhcq5Va4MCtCZcU7ptpsK8EO97hShKIHlRIZA130_provenance
a
np:Provenance
.
dgn-np:NP874721.RAf85nkajhcq5Va4MCtCZcU7ptpsK8EO97hShKIHlRIZA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP874721.RAf85nkajhcq5Va4MCtCZcU7ptpsK8EO97hShKIHlRIZA130_assertion
{
miriam-gene:6683
a
ncit:C16612
.
lld:C1858712
a
ncit:C7057
.
dgn-gda:DGN481176a1d0b4d8631155ba8dd155089b
sio:SIO_000628
miriam-gene:6683
,
lld:C1858712
;
a
sio:SIO_001121
.
}
dgn-np:NP874721.RAf85nkajhcq5Va4MCtCZcU7ptpsK8EO97hShKIHlRIZA130_provenance
{
dgn-np:NP874721.RAf85nkajhcq5Va4MCtCZcU7ptpsK8EO97hShKIHlRIZA130_assertion
dcterms:description
"[We report the clinical features of 12 families with autosomal dominant spastic paraplegia (ADSP) linked to the SPG4 locus on chromosome 2p, the major locus for this disorder that accounts for approximately 40% of the families.]. 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:8931574
;
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:NP874721.RAf85nkajhcq5Va4MCtCZcU7ptpsK8EO97hShKIHlRIZA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:54+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" .
}