@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP435385.RAfiqzW7p16TCXSNYwyq-_mawNELAePDy6tXmHTKz87Rg
> .
@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:NP435385.RAfiqzW7p16TCXSNYwyq-_mawNELAePDy6tXmHTKz87Rg130_head
{
this:
np:hasAssertion
dgn-np:NP435385.RAfiqzW7p16TCXSNYwyq-_mawNELAePDy6tXmHTKz87Rg130_assertion
;
np:hasProvenance
dgn-np:NP435385.RAfiqzW7p16TCXSNYwyq-_mawNELAePDy6tXmHTKz87Rg130_provenance
;
np:hasPublicationInfo
dgn-np:NP435385.RAfiqzW7p16TCXSNYwyq-_mawNELAePDy6tXmHTKz87Rg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP435385.RAfiqzW7p16TCXSNYwyq-_mawNELAePDy6tXmHTKz87Rg130_assertion
a
np:Assertion
.
dgn-np:NP435385.RAfiqzW7p16TCXSNYwyq-_mawNELAePDy6tXmHTKz87Rg130_provenance
a
np:Provenance
.
dgn-np:NP435385.RAfiqzW7p16TCXSNYwyq-_mawNELAePDy6tXmHTKz87Rg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP435385.RAfiqzW7p16TCXSNYwyq-_mawNELAePDy6tXmHTKz87Rg130_assertion
{
miriam-gene:10971
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGNa4e8b9a370154fbd7c42d811032df852
sio:SIO_000628
miriam-gene:10971
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP435385.RAfiqzW7p16TCXSNYwyq-_mawNELAePDy6tXmHTKz87Rg130_provenance
{
dgn-np:NP435385.RAfiqzW7p16TCXSNYwyq-_mawNELAePDy6tXmHTKz87Rg130_assertion
dcterms:description
"[We found a significant up-regulation of 1C5 (YWHAQ) in lumbar spinal cord from patients with sporadic ALS compared with controls, with the highest levels of expression being found in individuals with predominant lower motor neurone involvement.]. 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:11080204
;
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:NP435385.RAfiqzW7p16TCXSNYwyq-_mawNELAePDy6tXmHTKz87Rg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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" .
}