@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP357832.RA-FXKW4sea7cst4g5jB8dHcnXoeEg5D-dxbq4k3TMRZ0
> .
@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:NP357832.RA-FXKW4sea7cst4g5jB8dHcnXoeEg5D-dxbq4k3TMRZ0130_head
{
this:
np:hasAssertion
dgn-np:NP357832.RA-FXKW4sea7cst4g5jB8dHcnXoeEg5D-dxbq4k3TMRZ0130_assertion
;
np:hasProvenance
dgn-np:NP357832.RA-FXKW4sea7cst4g5jB8dHcnXoeEg5D-dxbq4k3TMRZ0130_provenance
;
np:hasPublicationInfo
dgn-np:NP357832.RA-FXKW4sea7cst4g5jB8dHcnXoeEg5D-dxbq4k3TMRZ0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP357832.RA-FXKW4sea7cst4g5jB8dHcnXoeEg5D-dxbq4k3TMRZ0130_assertion
a
np:Assertion
.
dgn-np:NP357832.RA-FXKW4sea7cst4g5jB8dHcnXoeEg5D-dxbq4k3TMRZ0130_provenance
a
np:Provenance
.
dgn-np:NP357832.RA-FXKW4sea7cst4g5jB8dHcnXoeEg5D-dxbq4k3TMRZ0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP357832.RA-FXKW4sea7cst4g5jB8dHcnXoeEg5D-dxbq4k3TMRZ0130_assertion
{
miriam-gene:6647
a
ncit:C16612
.
lld:C0085084
a
ncit:C7057
.
dgn-gda:DGNeb11f4fb00ab1740ef9cbf5142d888d5
sio:SIO_000628
miriam-gene:6647
,
lld:C0085084
;
a
sio:SIO_001121
.
}
dgn-np:NP357832.RA-FXKW4sea7cst4g5jB8dHcnXoeEg5D-dxbq4k3TMRZ0130_provenance
{
dgn-np:NP357832.RA-FXKW4sea7cst4g5jB8dHcnXoeEg5D-dxbq4k3TMRZ0130_assertion
dcterms:description
"[Transgenic mice that highly over-express a mutated human CuZn superoxide dismutase (SOD1) gene [gly93-->ala; TgN(SOD1-G93A)G1H line] found in some patients with familial ALS (FALS) have been shown to develop motor neuron disease that is characterized by motor neuron loss in the lumbar and cervical spinal regions and a progressive loss of motor activity.]. 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:9633809
;
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:NP357832.RA-FXKW4sea7cst4g5jB8dHcnXoeEg5D-dxbq4k3TMRZ0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:30+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" .
}