@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE
> .
@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:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_head
{
this:
np:hasAssertion
dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_assertion
;
np:hasProvenance
dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_provenance
;
np:hasPublicationInfo
dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_assertion
a
np:Assertion
.
dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_provenance
a
np:Provenance
.
dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_assertion
{
miriam-gene:7190
a
ncit:C16612
.
lld:C0037772
a
ncit:C7057
.
dgn-gda:DGNeb0e5d19d2ae123185692574c17ed54c
sio:SIO_000628
miriam-gene:7190
,
lld:C0037772
;
a
sio:SIO_001121
.
}
dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_provenance
{
dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_assertion
dcterms:description
"[HSP is classified according to the mode of inheritance, the HSP locus when known, and whether the spastic paraplegia syndrome occurs alone or is accompanied by additional neurologic or systemic abnormalities.]. 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:16469273
;
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:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:11+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" .
}