@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP184940.RAbvp6779zqPzSJxzHMuYNxRVx7z6wJtS9fl37wS_msho
> .
@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:NP184940.RAbvp6779zqPzSJxzHMuYNxRVx7z6wJtS9fl37wS_msho130_head
{
this:
np:hasAssertion
dgn-np:NP184940.RAbvp6779zqPzSJxzHMuYNxRVx7z6wJtS9fl37wS_msho130_assertion
;
np:hasProvenance
dgn-np:NP184940.RAbvp6779zqPzSJxzHMuYNxRVx7z6wJtS9fl37wS_msho130_provenance
;
np:hasPublicationInfo
dgn-np:NP184940.RAbvp6779zqPzSJxzHMuYNxRVx7z6wJtS9fl37wS_msho130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP184940.RAbvp6779zqPzSJxzHMuYNxRVx7z6wJtS9fl37wS_msho130_assertion
a
np:Assertion
.
dgn-np:NP184940.RAbvp6779zqPzSJxzHMuYNxRVx7z6wJtS9fl37wS_msho130_provenance
a
np:Provenance
.
dgn-np:NP184940.RAbvp6779zqPzSJxzHMuYNxRVx7z6wJtS9fl37wS_msho130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP184940.RAbvp6779zqPzSJxzHMuYNxRVx7z6wJtS9fl37wS_msho130_assertion
{
miriam-gene:6647
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN57db5f6e33388d72a3e4507d8320741e
sio:SIO_000628
miriam-gene:6647
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP184940.RAbvp6779zqPzSJxzHMuYNxRVx7z6wJtS9fl37wS_msho130_provenance
{
dgn-np:NP184940.RAbvp6779zqPzSJxzHMuYNxRVx7z6wJtS9fl37wS_msho130_assertion
dcterms:description
"[The fragmentation of the GA was identical to that previously reported in motor neurons of the spinal cord and motor cortex from patients with sporadic ALS and in transgenic mice expressing the G93A mutation of the gene encoding the Cu/Zn superoxide dismutase months before the onset of paralysis.]. 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:10727699
;
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:NP184940.RAbvp6779zqPzSJxzHMuYNxRVx7z6wJtS9fl37wS_msho130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:41+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" .
}