@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP549979.RA9wt3yrs9nIfrvC4XsUVFW4577XXo2cuXSHvqLTCtlYQ
> .
@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:NP549979.RA9wt3yrs9nIfrvC4XsUVFW4577XXo2cuXSHvqLTCtlYQ130_head
{
this:
np:hasAssertion
dgn-np:NP549979.RA9wt3yrs9nIfrvC4XsUVFW4577XXo2cuXSHvqLTCtlYQ130_assertion
;
np:hasProvenance
dgn-np:NP549979.RA9wt3yrs9nIfrvC4XsUVFW4577XXo2cuXSHvqLTCtlYQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP549979.RA9wt3yrs9nIfrvC4XsUVFW4577XXo2cuXSHvqLTCtlYQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP549979.RA9wt3yrs9nIfrvC4XsUVFW4577XXo2cuXSHvqLTCtlYQ130_assertion
a
np:Assertion
.
dgn-np:NP549979.RA9wt3yrs9nIfrvC4XsUVFW4577XXo2cuXSHvqLTCtlYQ130_provenance
a
np:Provenance
.
dgn-np:NP549979.RA9wt3yrs9nIfrvC4XsUVFW4577XXo2cuXSHvqLTCtlYQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP549979.RA9wt3yrs9nIfrvC4XsUVFW4577XXo2cuXSHvqLTCtlYQ130_assertion
{
miriam-gene:391104
a
ncit:C16612
.
lld:C0276379
a
ncit:C7057
.
dgn-gda:DGN39770d0c01b94cb3605ace64f30d5b35
sio:SIO_000628
miriam-gene:391104
,
lld:C0276379
;
a
sio:SIO_001121
.
}
dgn-np:NP549979.RA9wt3yrs9nIfrvC4XsUVFW4577XXo2cuXSHvqLTCtlYQ130_provenance
{
dgn-np:NP549979.RA9wt3yrs9nIfrvC4XsUVFW4577XXo2cuXSHvqLTCtlYQ130_assertion
dcterms:description
"[Blind-coded human serum panels were assembled from patients having recent SLEV, West Nile virus (WNV), Powassan virus, or La Crosse encephalitis virus infections to assess the sensitivity and specificity of assays with SLEV VLP or SMB antigen.]. 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:15472331
;
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:NP549979.RA9wt3yrs9nIfrvC4XsUVFW4577XXo2cuXSHvqLTCtlYQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:31+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" .
}