@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP30366.RAKPXzfZ10rx08vL39F3-Lxt52bJTb8ahImBudiT0ewvE
> .
@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:NP30366.RAKPXzfZ10rx08vL39F3-Lxt52bJTb8ahImBudiT0ewvE130_head
{
this:
np:hasAssertion
dgn-np:NP30366.RAKPXzfZ10rx08vL39F3-Lxt52bJTb8ahImBudiT0ewvE130_assertion
;
np:hasProvenance
dgn-np:NP30366.RAKPXzfZ10rx08vL39F3-Lxt52bJTb8ahImBudiT0ewvE130_provenance
;
np:hasPublicationInfo
dgn-np:NP30366.RAKPXzfZ10rx08vL39F3-Lxt52bJTb8ahImBudiT0ewvE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP30366.RAKPXzfZ10rx08vL39F3-Lxt52bJTb8ahImBudiT0ewvE130_assertion
a
np:Assertion
.
dgn-np:NP30366.RAKPXzfZ10rx08vL39F3-Lxt52bJTb8ahImBudiT0ewvE130_provenance
a
np:Provenance
.
dgn-np:NP30366.RAKPXzfZ10rx08vL39F3-Lxt52bJTb8ahImBudiT0ewvE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP30366.RAKPXzfZ10rx08vL39F3-Lxt52bJTb8ahImBudiT0ewvE130_assertion
{
miriam-gene:6647
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN205bf082c28a84bfd4bee4d45be1b693
sio:SIO_000628
miriam-gene:6647
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP30366.RAKPXzfZ10rx08vL39F3-Lxt52bJTb8ahImBudiT0ewvE130_provenance
{
dgn-np:NP30366.RAKPXzfZ10rx08vL39F3-Lxt52bJTb8ahImBudiT0ewvE130_assertion
dcterms:description
"[Despite the more limited amelioration of disease than expected, the effect of the knockdown on disease supports the value of this approach in FALS patients and asymptomatic individuals with SOD1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:20132483
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP30366.RAKPXzfZ10rx08vL39F3-Lxt52bJTb8ahImBudiT0ewvE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:13+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" .
}