@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP316398.RAmy_HZkeuEJ0qFrFo28i9_Lf1jilOpaJCrCp-pEV6EgE
> .
@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:NP316398.RAmy_HZkeuEJ0qFrFo28i9_Lf1jilOpaJCrCp-pEV6EgE130_head
{
this:
np:hasAssertion
dgn-np:NP316398.RAmy_HZkeuEJ0qFrFo28i9_Lf1jilOpaJCrCp-pEV6EgE130_assertion
;
np:hasProvenance
dgn-np:NP316398.RAmy_HZkeuEJ0qFrFo28i9_Lf1jilOpaJCrCp-pEV6EgE130_provenance
;
np:hasPublicationInfo
dgn-np:NP316398.RAmy_HZkeuEJ0qFrFo28i9_Lf1jilOpaJCrCp-pEV6EgE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP316398.RAmy_HZkeuEJ0qFrFo28i9_Lf1jilOpaJCrCp-pEV6EgE130_assertion
a
np:Assertion
.
dgn-np:NP316398.RAmy_HZkeuEJ0qFrFo28i9_Lf1jilOpaJCrCp-pEV6EgE130_provenance
a
np:Provenance
.
dgn-np:NP316398.RAmy_HZkeuEJ0qFrFo28i9_Lf1jilOpaJCrCp-pEV6EgE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP316398.RAmy_HZkeuEJ0qFrFo28i9_Lf1jilOpaJCrCp-pEV6EgE130_assertion
{
miriam-gene:118429
a
ncit:C16612
.
lld:C0007682
a
ncit:C7057
.
dgn-gda:DGN0cf30d4637710915d7a00147e564caa5
sio:SIO_000628
miriam-gene:118429
,
lld:C0007682
;
a
sio:SIO_001121
.
}
dgn-np:NP316398.RAmy_HZkeuEJ0qFrFo28i9_Lf1jilOpaJCrCp-pEV6EgE130_provenance
{
dgn-np:NP316398.RAmy_HZkeuEJ0qFrFo28i9_Lf1jilOpaJCrCp-pEV6EgE130_assertion
dcterms:description
"[In order to obtain a useful and readily applicable in situ hybridization (ISH) protocol for progressive central nervous system (CNS) diseases of unknown etiology that are possibly due to persistent viral infection, known and well described diseases were studied, namely, progressive multifocal leukoencephalopathy (PML) and subacute sclerosing panencephalitis (SSPE).]. 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:3746947
;
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:NP316398.RAmy_HZkeuEJ0qFrFo28i9_Lf1jilOpaJCrCp-pEV6EgE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:01+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" .
}