@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP215819.RA8-tV3MNHlDSgWO351N_fjf_1PdCB1Co0ND0uvnmjZvk
> .
@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:NP215819.RA8-tV3MNHlDSgWO351N_fjf_1PdCB1Co0ND0uvnmjZvk130_head
{
this:
np:hasAssertion
dgn-np:NP215819.RA8-tV3MNHlDSgWO351N_fjf_1PdCB1Co0ND0uvnmjZvk130_assertion
;
np:hasProvenance
dgn-np:NP215819.RA8-tV3MNHlDSgWO351N_fjf_1PdCB1Co0ND0uvnmjZvk130_provenance
;
np:hasPublicationInfo
dgn-np:NP215819.RA8-tV3MNHlDSgWO351N_fjf_1PdCB1Co0ND0uvnmjZvk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP215819.RA8-tV3MNHlDSgWO351N_fjf_1PdCB1Co0ND0uvnmjZvk130_assertion
a
np:Assertion
.
dgn-np:NP215819.RA8-tV3MNHlDSgWO351N_fjf_1PdCB1Co0ND0uvnmjZvk130_provenance
a
np:Provenance
.
dgn-np:NP215819.RA8-tV3MNHlDSgWO351N_fjf_1PdCB1Co0ND0uvnmjZvk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP215819.RA8-tV3MNHlDSgWO351N_fjf_1PdCB1Co0ND0uvnmjZvk130_assertion
{
miriam-gene:4948
a
ncit:C16612
.
lld:C0034152
a
ncit:C7057
.
dgn-gda:DGN04d72737b6a41e98cbb6f29b228a6695
sio:SIO_000628
miriam-gene:4948
,
lld:C0034152
;
a
sio:SIO_001121
.
}
dgn-np:NP215819.RA8-tV3MNHlDSgWO351N_fjf_1PdCB1Co0ND0uvnmjZvk130_provenance
{
dgn-np:NP215819.RA8-tV3MNHlDSgWO351N_fjf_1PdCB1Co0ND0uvnmjZvk130_assertion
dcterms:description
"[We tested whether 1) progressive spastic paraparesis, in addition to PED, as described in DYT9, and 2) autosomal dominant forms of hereditary spastic paraparesis (HSP) without PED are caused by SLC2A1 defects.]. 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:21832227
;
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:NP215819.RA8-tV3MNHlDSgWO351N_fjf_1PdCB1Co0ND0uvnmjZvk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:59+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" .
}