@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_head
{
this:
np:hasAssertion
dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_assertion
;
np:hasProvenance
dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_provenance
;
np:hasPublicationInfo
dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_assertion
a
np:Assertion
.
dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_provenance
a
np:Provenance
.
dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_assertion
{
miriam-gene:6647
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGNfff7d35e660088540f6330b83a315a13
sio:SIO_000628
miriam-gene:6647
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_provenance
{
dgn-np:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_assertion
dcterms:description
"[Focusing on amyotrophic lateral sclerosis (ALS), especially disease caused by dominant mutations in Cu/Zn superoxide dismutase (SOD1), we review here the evidence that it is the convergence of damage developed within multiple cell types, including within neighboring nonneuronal supporting cells, which is crucial to neuronal dysfunction.]. 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:19951898
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP778650.RAH8rwAkjF6iNPdzlvO0wW6_L5To1ID_kLO-rokF2pVHc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:38+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}