@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP141609.RA8kvv8Rni6wlgVaaka8sms4Zkl8lRDLRnjPTgEuYGt_c
> .
@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:NP141609.RA8kvv8Rni6wlgVaaka8sms4Zkl8lRDLRnjPTgEuYGt_c130_head
{
this:
np:hasAssertion
dgn-np:NP141609.RA8kvv8Rni6wlgVaaka8sms4Zkl8lRDLRnjPTgEuYGt_c130_assertion
;
np:hasProvenance
dgn-np:NP141609.RA8kvv8Rni6wlgVaaka8sms4Zkl8lRDLRnjPTgEuYGt_c130_provenance
;
np:hasPublicationInfo
dgn-np:NP141609.RA8kvv8Rni6wlgVaaka8sms4Zkl8lRDLRnjPTgEuYGt_c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP141609.RA8kvv8Rni6wlgVaaka8sms4Zkl8lRDLRnjPTgEuYGt_c130_assertion
a
np:Assertion
.
dgn-np:NP141609.RA8kvv8Rni6wlgVaaka8sms4Zkl8lRDLRnjPTgEuYGt_c130_provenance
a
np:Provenance
.
dgn-np:NP141609.RA8kvv8Rni6wlgVaaka8sms4Zkl8lRDLRnjPTgEuYGt_c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP141609.RA8kvv8Rni6wlgVaaka8sms4Zkl8lRDLRnjPTgEuYGt_c130_assertion
{
miriam-gene:23503
a
ncit:C16612
.
lld:C0037773
a
ncit:C7057
.
dgn-gda:DGNd48cc9e6de1609f5d6fbb1b924d08b57
sio:SIO_000628
miriam-gene:23503
,
lld:C0037773
;
a
sio:SIO_001122
.
}
dgn-np:NP141609.RA8kvv8Rni6wlgVaaka8sms4Zkl8lRDLRnjPTgEuYGt_c130_provenance
{
dgn-np:NP141609.RA8kvv8Rni6wlgVaaka8sms4Zkl8lRDLRnjPTgEuYGt_c130_assertion
dcterms:description
"[phenotypic heterogeneity of SPG15 in which mental retardation or cognitive deterioration, but not all other signs of Kjellin syndrome, are associated with hereditary spastic paraplegia and significantly reduces the SPG15 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:17661097
;
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:NP141609.RA8kvv8Rni6wlgVaaka8sms4Zkl8lRDLRnjPTgEuYGt_c130_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" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}