@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP510738.RAb86C-J0LL0Bz3BhE2BICqcVnMqvD2HQ-1UjeM-xHKvc
> .
@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:NP510738.RAb86C-J0LL0Bz3BhE2BICqcVnMqvD2HQ-1UjeM-xHKvc130_head
{
this:
np:hasAssertion
dgn-np:NP510738.RAb86C-J0LL0Bz3BhE2BICqcVnMqvD2HQ-1UjeM-xHKvc130_assertion
;
np:hasProvenance
dgn-np:NP510738.RAb86C-J0LL0Bz3BhE2BICqcVnMqvD2HQ-1UjeM-xHKvc130_provenance
;
np:hasPublicationInfo
dgn-np:NP510738.RAb86C-J0LL0Bz3BhE2BICqcVnMqvD2HQ-1UjeM-xHKvc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP510738.RAb86C-J0LL0Bz3BhE2BICqcVnMqvD2HQ-1UjeM-xHKvc130_assertion
a
np:Assertion
.
dgn-np:NP510738.RAb86C-J0LL0Bz3BhE2BICqcVnMqvD2HQ-1UjeM-xHKvc130_provenance
a
np:Provenance
.
dgn-np:NP510738.RAb86C-J0LL0Bz3BhE2BICqcVnMqvD2HQ-1UjeM-xHKvc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP510738.RAb86C-J0LL0Bz3BhE2BICqcVnMqvD2HQ-1UjeM-xHKvc130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0007099
a
ncit:C7057
.
dgn-gda:DGN95720362fb3703d4a64d5828093734a7
sio:SIO_000628
miriam-gene:1437
,
lld:C0007099
;
a
sio:SIO_001121
.
}
dgn-np:NP510738.RAb86C-J0LL0Bz3BhE2BICqcVnMqvD2HQ-1UjeM-xHKvc130_provenance
{
dgn-np:NP510738.RAb86C-J0LL0Bz3BhE2BICqcVnMqvD2HQ-1UjeM-xHKvc130_assertion
dcterms:description
"[The prevalence of JCV DNA was analyzed in CSF and plasma from 217 patients with MS, 86 patients with clinically isolated syndrome (CIS), and 212 patients with other neurological diseases (OND).]. 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:18805840
;
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:NP510738.RAb86C-J0LL0Bz3BhE2BICqcVnMqvD2HQ-1UjeM-xHKvc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}