@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP228101.RAe-rSkbj5YQMaQGkZ_UAw5jU9zjcZQZBDZIBcq3xQKKQ
> .
@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:NP228101.RAe-rSkbj5YQMaQGkZ_UAw5jU9zjcZQZBDZIBcq3xQKKQ130_head
{
this:
np:hasAssertion
dgn-np:NP228101.RAe-rSkbj5YQMaQGkZ_UAw5jU9zjcZQZBDZIBcq3xQKKQ130_assertion
;
np:hasProvenance
dgn-np:NP228101.RAe-rSkbj5YQMaQGkZ_UAw5jU9zjcZQZBDZIBcq3xQKKQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP228101.RAe-rSkbj5YQMaQGkZ_UAw5jU9zjcZQZBDZIBcq3xQKKQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP228101.RAe-rSkbj5YQMaQGkZ_UAw5jU9zjcZQZBDZIBcq3xQKKQ130_assertion
a
np:Assertion
.
dgn-np:NP228101.RAe-rSkbj5YQMaQGkZ_UAw5jU9zjcZQZBDZIBcq3xQKKQ130_provenance
a
np:Provenance
.
dgn-np:NP228101.RAe-rSkbj5YQMaQGkZ_UAw5jU9zjcZQZBDZIBcq3xQKKQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP228101.RAe-rSkbj5YQMaQGkZ_UAw5jU9zjcZQZBDZIBcq3xQKKQ130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0023524
a
ncit:C7057
.
dgn-gda:DGN91e3adf6d744fd567b861c2544acf6d1
sio:SIO_000628
miriam-gene:1437
,
lld:C0023524
;
a
sio:SIO_001121
.
}
dgn-np:NP228101.RAe-rSkbj5YQMaQGkZ_UAw5jU9zjcZQZBDZIBcq3xQKKQ130_provenance
{
dgn-np:NP228101.RAe-rSkbj5YQMaQGkZ_UAw5jU9zjcZQZBDZIBcq3xQKKQ130_assertion
dcterms:description
"[In order to provide more insight to PML pathogenesis and identify potential prognostic markers, seven cerebrospinal fluid (CSF) samples and four brain autopsy samples were collected from patients afflicted with PML with different clinical courses (fast- and slow-progressing), and the JCV VP1 coding region was amplified, cloned, and sequenced.]. 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:19043822
;
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:NP228101.RAe-rSkbj5YQMaQGkZ_UAw5jU9zjcZQZBDZIBcq3xQKKQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}