@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP391760.RAABYR8THc3bMFkM-faFhVVrH-C-ndX1LoMIs8ODvzdC8
> .
@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:NP391760.RAABYR8THc3bMFkM-faFhVVrH-C-ndX1LoMIs8ODvzdC8130_head
{
this:
np:hasAssertion
dgn-np:NP391760.RAABYR8THc3bMFkM-faFhVVrH-C-ndX1LoMIs8ODvzdC8130_assertion
;
np:hasProvenance
dgn-np:NP391760.RAABYR8THc3bMFkM-faFhVVrH-C-ndX1LoMIs8ODvzdC8130_provenance
;
np:hasPublicationInfo
dgn-np:NP391760.RAABYR8THc3bMFkM-faFhVVrH-C-ndX1LoMIs8ODvzdC8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP391760.RAABYR8THc3bMFkM-faFhVVrH-C-ndX1LoMIs8ODvzdC8130_assertion
a
np:Assertion
.
dgn-np:NP391760.RAABYR8THc3bMFkM-faFhVVrH-C-ndX1LoMIs8ODvzdC8130_provenance
a
np:Provenance
.
dgn-np:NP391760.RAABYR8THc3bMFkM-faFhVVrH-C-ndX1LoMIs8ODvzdC8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP391760.RAABYR8THc3bMFkM-faFhVVrH-C-ndX1LoMIs8ODvzdC8130_assertion
{
miriam-gene:6687
a
ncit:C16612
.
lld:C0034152
a
ncit:C7057
.
dgn-gda:DGN7df5eb5ac5f20e60082a6bd6a41dcdfd
sio:SIO_000628
miriam-gene:6687
,
lld:C0034152
;
a
sio:SIO_001121
.
}
dgn-np:NP391760.RAABYR8THc3bMFkM-faFhVVrH-C-ndX1LoMIs8ODvzdC8130_provenance
{
dgn-np:NP391760.RAABYR8THc3bMFkM-faFhVVrH-C-ndX1LoMIs8ODvzdC8130_assertion
dcterms:description
"[Following the association of hereditary spastic paraparesis (HSP) with mutation in the paraplegin gene (SPG7) and mitochondrial dysfunction, we wished to investigate whether mitochondrial dysfunction might be associated with other forms of HSP.]. 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:12634509
;
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:NP391760.RAABYR8THc3bMFkM-faFhVVrH-C-ndX1LoMIs8ODvzdC8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:53+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" .
}