@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc
> .
@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:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_head
{
this:
np:hasAssertion
dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_assertion
;
np:hasProvenance
dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_provenance
;
np:hasPublicationInfo
dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_assertion
a
np:Assertion
.
dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_provenance
a
np:Provenance
.
dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_assertion
{
miriam-gene:1917
a
ncit:C16612
.
lld:C0235394
a
ncit:C7057
.
dgn-gda:DGN0ebc938c064d635e38c2caf0806e0b98
sio:SIO_000628
miriam-gene:1917
,
lld:C0235394
;
a
sio:SIO_001121
.
}
dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_provenance
{
dgn-np:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_assertion
dcterms:description
"[We conclude that spontaneous failure of eEF1A2 expression in the wasted mutant first triggers gliosis in spinal cord and retraction of motor nerve terminals in muscle, and then motor neuron pathology and death.]. 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:15835265
;
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:NP288081.RAABzCsHMSlFgThXmZ6tKSkp9O72ouTXhltzV0i0iXQYc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:44+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" .
}