@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8
> .
@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:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_head
{
this:
np:hasAssertion
dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_assertion
;
np:hasProvenance
dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_provenance
;
np:hasPublicationInfo
dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_assertion
a
np:Assertion
.
dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_provenance
a
np:Provenance
.
dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_assertion
{
miriam-gene:6647
a
ncit:C16612
.
lld:C1883552
a
ncit:C7057
.
dgn-gda:DGNb75f77f158ec82f440a118be15e27282
sio:SIO_000628
miriam-gene:6647
,
lld:C1883552
;
a
sio:SIO_001121
.
}
dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_provenance
{
dgn-np:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_assertion
dcterms:description
"[Based on the temporal correlation of these impairments with the onset of motor weakness and the appearance of NF inclusions and vacuoles in vulnerable motor neurons, the latter lesions may be the proximal cause of motor neuron dysfunction and degeneration in the G93A mice and in FALS patients with SOD1 mutations.]. 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:9382875
;
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:NP612810.RAiYPXrrdYdHBKJ9pSyzkAEXric01zhGwDj1iMiLcSDN8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:10+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" .
}