@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP545767.RA8rydPFc_AiHIpwCAhSHYpZ1S3DozhAh6BcW-DtzFbLU
> .
@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:NP545767.RA8rydPFc_AiHIpwCAhSHYpZ1S3DozhAh6BcW-DtzFbLU130_head
{
this:
np:hasAssertion
dgn-np:NP545767.RA8rydPFc_AiHIpwCAhSHYpZ1S3DozhAh6BcW-DtzFbLU130_assertion
;
np:hasProvenance
dgn-np:NP545767.RA8rydPFc_AiHIpwCAhSHYpZ1S3DozhAh6BcW-DtzFbLU130_provenance
;
np:hasPublicationInfo
dgn-np:NP545767.RA8rydPFc_AiHIpwCAhSHYpZ1S3DozhAh6BcW-DtzFbLU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP545767.RA8rydPFc_AiHIpwCAhSHYpZ1S3DozhAh6BcW-DtzFbLU130_assertion
a
np:Assertion
.
dgn-np:NP545767.RA8rydPFc_AiHIpwCAhSHYpZ1S3DozhAh6BcW-DtzFbLU130_provenance
a
np:Provenance
.
dgn-np:NP545767.RA8rydPFc_AiHIpwCAhSHYpZ1S3DozhAh6BcW-DtzFbLU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP545767.RA8rydPFc_AiHIpwCAhSHYpZ1S3DozhAh6BcW-DtzFbLU130_assertion
{
miriam-gene:94081
a
ncit:C16612
.
lld:C0034152
a
ncit:C7057
.
dgn-gda:DGNa3613ae01ae0069914bfa408161cbff0
sio:SIO_000628
miriam-gene:94081
,
lld:C0034152
;
a
sio:SIO_001121
.
}
dgn-np:NP545767.RA8rydPFc_AiHIpwCAhSHYpZ1S3DozhAh6BcW-DtzFbLU130_provenance
{
dgn-np:NP545767.RA8rydPFc_AiHIpwCAhSHYpZ1S3DozhAh6BcW-DtzFbLU130_assertion
dcterms:description
"[Hereditary spastic paraplegia (HSP) with thin corpus callosum (TCC) is an autosomal recessive form of complicated HSP mainly characterized by slowly progressive spastic paraparesis and mental deterioration beginning in the second decade of life.]. 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:16682547
;
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:NP545767.RA8rydPFc_AiHIpwCAhSHYpZ1S3DozhAh6BcW-DtzFbLU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:29+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" .
}