@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o
> .
@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:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_head
{
this:
np:hasAssertion
dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_assertion
;
np:hasProvenance
dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_provenance
;
np:hasPublicationInfo
dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_assertion
a
np:Assertion
.
dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_provenance
a
np:Provenance
.
dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C1852467
a
ncit:C7057
.
dgn-gda:DGNd8dc14b6cc609dc242cae8ef32212882
sio:SIO_000628
miriam-gene:3918
,
lld:C1852467
;
a
sio:SIO_001121
.
}
dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_provenance
{
dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_assertion
dcterms:description
"[The increase in CSF levels of lactate dehydrogenase (LDH), glucose-6-phosphate isomerase (G6PI), and fructose-bisphosphate aldolase A (ALDOA) were validated on a larger group of sCJD patients including three possible codon 129 polymorphism carriers and three control groups consisting of nondemented, neurological cases as well as patients suffering from Alzheimer's disease or vascular dementia.]. 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:20866111
;
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:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:04+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" .
}