@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U
> .
@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:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_head
{
this:
np:hasAssertion
dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_assertion
;
np:hasProvenance
dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_provenance
;
np:hasPublicationInfo
dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_assertion
a
np:Assertion
.
dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_provenance
a
np:Provenance
.
dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_assertion
{
miriam-gene:23435
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN66b06cd238c16a7f0587084568934590
sio:SIO_000628
miriam-gene:23435
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_provenance
{
dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_assertion
dcterms:description
"[In conclusion, this report contributes to the demonstration of the causative role of the TARDBP gene in ALS pathogenesis and indicates that mutations may affect the stability of the protein even in nonneuronal tissues.]. 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:19224587
;
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:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}