@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP771132.RA6SIUtFDOS5zPe6BxF3WksAE1GUOwn2n-zGMYKQ5y1d4
> .
@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:NP771132.RA6SIUtFDOS5zPe6BxF3WksAE1GUOwn2n-zGMYKQ5y1d4130_head
{
this:
np:hasAssertion
dgn-np:NP771132.RA6SIUtFDOS5zPe6BxF3WksAE1GUOwn2n-zGMYKQ5y1d4130_assertion
;
np:hasProvenance
dgn-np:NP771132.RA6SIUtFDOS5zPe6BxF3WksAE1GUOwn2n-zGMYKQ5y1d4130_provenance
;
np:hasPublicationInfo
dgn-np:NP771132.RA6SIUtFDOS5zPe6BxF3WksAE1GUOwn2n-zGMYKQ5y1d4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP771132.RA6SIUtFDOS5zPe6BxF3WksAE1GUOwn2n-zGMYKQ5y1d4130_assertion
a
np:Assertion
.
dgn-np:NP771132.RA6SIUtFDOS5zPe6BxF3WksAE1GUOwn2n-zGMYKQ5y1d4130_provenance
a
np:Provenance
.
dgn-np:NP771132.RA6SIUtFDOS5zPe6BxF3WksAE1GUOwn2n-zGMYKQ5y1d4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP771132.RA6SIUtFDOS5zPe6BxF3WksAE1GUOwn2n-zGMYKQ5y1d4130_assertion
{
miriam-gene:3798
a
ncit:C16612
.
lld:C0037772
a
ncit:C7057
.
dgn-gda:DGNb7f12879aaf1def89fd2e43ef98aba53
sio:SIO_000628
miriam-gene:3798
,
lld:C0037772
;
a
sio:SIO_001121
.
}
dgn-np:NP771132.RA6SIUtFDOS5zPe6BxF3WksAE1GUOwn2n-zGMYKQ5y1d4130_provenance
{
dgn-np:NP771132.RA6SIUtFDOS5zPe6BxF3WksAE1GUOwn2n-zGMYKQ5y1d4130_assertion
dcterms:description
"[In conclusion, these data confirm the presence of SPG10 (chromosome 12), potentially reduce the minimum candidate region for SPG12 (chromosome 19q), and suggest there is at least one additional autosomal dominant SPG locus.]. 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:11354831
;
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:NP771132.RA6SIUtFDOS5zPe6BxF3WksAE1GUOwn2n-zGMYKQ5y1d4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:46+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" .
}