@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE
> .
@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:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_head
{
this:
np:hasAssertion
dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_assertion
;
np:hasProvenance
dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_provenance
;
np:hasPublicationInfo
dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_assertion
a
np:Assertion
.
dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_provenance
a
np:Provenance
.
dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_assertion
{
miriam-gene:6992
a
ncit:C16612
.
lld:C0023264
a
ncit:C7057
.
dgn-gda:DGN1e97ad083669fe6b6f339b29dd2e8203
sio:SIO_000628
miriam-gene:6992
,
lld:C0023264
;
a
sio:SIO_001121
.
}
dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_provenance
{
dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_assertion
dcterms:description
"[From clinical evidence these subjects were divided into five groups: (1) necropsy-proved cases of subacute necrotising encephalomyelopathy, (2) cases positive for urinary thiamine pyrophosphate: adenosine triphosphate phosphotransferase inhibitor, (3) clinically likely cases of subacute necrotising encephalomyelopathy (patients still alive, or on whom no necropsy was performed), (4) cases diagnosed as diseases other than subacute necrotising encephalomyelopathy (control group), (5) cases for which no diagnosis had been made.]. 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:7436444
;
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:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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" .
}