@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP525017.RA0ZXMeLHjMW1LTfgcqNV9hszgKhCCwoJjAuSa1NOy9BA
> .
@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:NP525017.RA0ZXMeLHjMW1LTfgcqNV9hszgKhCCwoJjAuSa1NOy9BA130_head
{
this:
np:hasAssertion
dgn-np:NP525017.RA0ZXMeLHjMW1LTfgcqNV9hszgKhCCwoJjAuSa1NOy9BA130_assertion
;
np:hasProvenance
dgn-np:NP525017.RA0ZXMeLHjMW1LTfgcqNV9hszgKhCCwoJjAuSa1NOy9BA130_provenance
;
np:hasPublicationInfo
dgn-np:NP525017.RA0ZXMeLHjMW1LTfgcqNV9hszgKhCCwoJjAuSa1NOy9BA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP525017.RA0ZXMeLHjMW1LTfgcqNV9hszgKhCCwoJjAuSa1NOy9BA130_assertion
a
np:Assertion
.
dgn-np:NP525017.RA0ZXMeLHjMW1LTfgcqNV9hszgKhCCwoJjAuSa1NOy9BA130_provenance
a
np:Provenance
.
dgn-np:NP525017.RA0ZXMeLHjMW1LTfgcqNV9hszgKhCCwoJjAuSa1NOy9BA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP525017.RA0ZXMeLHjMW1LTfgcqNV9hszgKhCCwoJjAuSa1NOy9BA130_assertion
{
miriam-gene:6647
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN33f90fd015beac54307cc3f1a09a8d9d
sio:SIO_000628
miriam-gene:6647
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP525017.RA0ZXMeLHjMW1LTfgcqNV9hszgKhCCwoJjAuSa1NOy9BA130_provenance
{
dgn-np:NP525017.RA0ZXMeLHjMW1LTfgcqNV9hszgKhCCwoJjAuSa1NOy9BA130_assertion
dcterms:description
"[While it may be that FALS is a consequence of loss of SOD1 function, it is also possible that motor neuron death in this dominantly inherited disease occurs because the mutations confer an additional, cytotoxic function on the SOD1 protein.]. 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:7951249
;
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:NP525017.RA0ZXMeLHjMW1LTfgcqNV9hszgKhCCwoJjAuSa1NOy9BA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:15+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" .
}