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http://rdf.disgenet.org/nanopublications.trig#NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_assertion
a
np:Assertion
.
dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_provenance
a
np:Provenance
.
dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_publicationInfo
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{
miriam-gene:613
a
ncit:C16612
.
lld:C1862939
a
ncit:C7057
.
dgn-gda:DGN3021116c2c462b52ac9dcc7c4b531d25
sio:SIO_000628
miriam-gene:613
,
lld:C1862939
;
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.
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dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_provenance
{
dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_assertion
dcterms:description
"[To clarify the neuropathological significance of the deposition of N(epsilon)-carboxymethyl lysine (CML), an advanced glycation endproduct, in astrocytic hyaline inclusions in familial amyotrophic lateral sclerosis (FALS), autopsy specimens from five members of two different families who had the superoxide dismutase 1 (SOD1) gene mutations were analysed.]. 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:10090673
;
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 .
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dgn-np:NP485009.RAUHxoj-DKXUwE0zIwH9ynMUgFt_Mt05SOytozUWJXMWM130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
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> , <
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> , <
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> ;
pav:createdBy
<
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