@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP268765.RAF0ZElX4_hoL0_-T5dawGmzGzh5Jj5JqGOsv6ahUAkQE
> .
@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:NP268765.RAF0ZElX4_hoL0_-T5dawGmzGzh5Jj5JqGOsv6ahUAkQE130_head
{
this:
np:hasAssertion
dgn-np:NP268765.RAF0ZElX4_hoL0_-T5dawGmzGzh5Jj5JqGOsv6ahUAkQE130_assertion
;
np:hasProvenance
dgn-np:NP268765.RAF0ZElX4_hoL0_-T5dawGmzGzh5Jj5JqGOsv6ahUAkQE130_provenance
;
np:hasPublicationInfo
dgn-np:NP268765.RAF0ZElX4_hoL0_-T5dawGmzGzh5Jj5JqGOsv6ahUAkQE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP268765.RAF0ZElX4_hoL0_-T5dawGmzGzh5Jj5JqGOsv6ahUAkQE130_assertion
a
np:Assertion
.
dgn-np:NP268765.RAF0ZElX4_hoL0_-T5dawGmzGzh5Jj5JqGOsv6ahUAkQE130_provenance
a
np:Provenance
.
dgn-np:NP268765.RAF0ZElX4_hoL0_-T5dawGmzGzh5Jj5JqGOsv6ahUAkQE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP268765.RAF0ZElX4_hoL0_-T5dawGmzGzh5Jj5JqGOsv6ahUAkQE130_assertion
{
miriam-gene:30811
a
ncit:C16612
.
lld:C0877221
a
ncit:C7057
.
dgn-gda:DGN9bd632c9672204d10093b39711251f48
sio:SIO_000628
miriam-gene:30811
,
lld:C0877221
;
a
sio:SIO_001121
.
}
dgn-np:NP268765.RAF0ZElX4_hoL0_-T5dawGmzGzh5Jj5JqGOsv6ahUAkQE130_provenance
{
dgn-np:NP268765.RAF0ZElX4_hoL0_-T5dawGmzGzh5Jj5JqGOsv6ahUAkQE130_assertion
dcterms:description
"[Since its discovery, human parvovirus B19 (B19V), now termed erythrovirus, has been associated with many clinical situations (neurological and myocardium infections, persistent B19V DNAemia) in addition to the prototype clinical manifestations, i.e., erythema infectiosum and erythroblastopenia crisis.]. 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:20631151
;
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:NP268765.RAF0ZElX4_hoL0_-T5dawGmzGzh5Jj5JqGOsv6ahUAkQE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:30+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" .
}