@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP855598.RAPiuSjOWok51MHzqVuibJLgXTNN7vZPnsox00Gvzk9xk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP855598.RAPiuSjOWok51MHzqVuibJLgXTNN7vZPnsox00Gvzk9xk130_head
{
this:
np:hasAssertion
dgn-np:NP855598.RAPiuSjOWok51MHzqVuibJLgXTNN7vZPnsox00Gvzk9xk130_assertion
;
np:hasProvenance
dgn-np:NP855598.RAPiuSjOWok51MHzqVuibJLgXTNN7vZPnsox00Gvzk9xk130_provenance
;
np:hasPublicationInfo
dgn-np:NP855598.RAPiuSjOWok51MHzqVuibJLgXTNN7vZPnsox00Gvzk9xk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP855598.RAPiuSjOWok51MHzqVuibJLgXTNN7vZPnsox00Gvzk9xk130_assertion
a
np:Assertion
.
dgn-np:NP855598.RAPiuSjOWok51MHzqVuibJLgXTNN7vZPnsox00Gvzk9xk130_provenance
a
np:Provenance
.
dgn-np:NP855598.RAPiuSjOWok51MHzqVuibJLgXTNN7vZPnsox00Gvzk9xk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP855598.RAPiuSjOWok51MHzqVuibJLgXTNN7vZPnsox00Gvzk9xk130_assertion
{
miriam-gene:10908
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN59b60186149fb315b0e4925d215de965
sio:SIO_000628
miriam-gene:10908
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP855598.RAPiuSjOWok51MHzqVuibJLgXTNN7vZPnsox00Gvzk9xk130_provenance
{
dgn-np:NP855598.RAPiuSjOWok51MHzqVuibJLgXTNN7vZPnsox00Gvzk9xk130_assertion
dcterms:description
"[Disease-specific, nonconserved NTE mutations in unrelated MND patients indicates NTE's importance in maintaining axonal integrity, raises the possibility that NTE pathway disturbances contribute to other MNDs including ALS, and supports the role of NTE abnormalities in axonopathy produced by neuropathic OP compounds.]. 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:18313024
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP855598.RAPiuSjOWok51MHzqVuibJLgXTNN7vZPnsox00Gvzk9xk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:19+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}