@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP445303.RAliHTW9-zIXWtHkR53tJ_uASCC9kQpG11tJwWLlvrLsI
> .
@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:NP445303.RAliHTW9-zIXWtHkR53tJ_uASCC9kQpG11tJwWLlvrLsI130_head
{
this:
np:hasAssertion
dgn-np:NP445303.RAliHTW9-zIXWtHkR53tJ_uASCC9kQpG11tJwWLlvrLsI130_assertion
;
np:hasProvenance
dgn-np:NP445303.RAliHTW9-zIXWtHkR53tJ_uASCC9kQpG11tJwWLlvrLsI130_provenance
;
np:hasPublicationInfo
dgn-np:NP445303.RAliHTW9-zIXWtHkR53tJ_uASCC9kQpG11tJwWLlvrLsI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP445303.RAliHTW9-zIXWtHkR53tJ_uASCC9kQpG11tJwWLlvrLsI130_assertion
a
np:Assertion
.
dgn-np:NP445303.RAliHTW9-zIXWtHkR53tJ_uASCC9kQpG11tJwWLlvrLsI130_provenance
a
np:Provenance
.
dgn-np:NP445303.RAliHTW9-zIXWtHkR53tJ_uASCC9kQpG11tJwWLlvrLsI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP445303.RAliHTW9-zIXWtHkR53tJ_uASCC9kQpG11tJwWLlvrLsI130_assertion
{
miriam-gene:4485
a
ncit:C16612
.
lld:C0338451
a
ncit:C7057
.
dgn-gda:DGNcc7e57ddd0e69a7c5acb75efb5fc4a08
sio:SIO_000628
miriam-gene:4485
,
lld:C0338451
;
a
sio:SIO_001121
.
}
dgn-np:NP445303.RAliHTW9-zIXWtHkR53tJ_uASCC9kQpG11tJwWLlvrLsI130_provenance
{
dgn-np:NP445303.RAliHTW9-zIXWtHkR53tJ_uASCC9kQpG11tJwWLlvrLsI130_assertion
dcterms:description
"[Genetic defects in MSP implicate a range of biological mechanisms including RNA processing and protein homeostasis, both with potential relevance to the pathobiology of more common MNDs such as amyotrophic lateral sclerosis (ALS) and providing an additional link between ALS and FTD.]. 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:23635965
;
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:NP445303.RAliHTW9-zIXWtHkR53tJ_uASCC9kQpG11tJwWLlvrLsI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:25+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" .
}