@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP235012.RAvu6YtB1LENfdh5KHJgRm1LnDARFiYKergSlWJbKrsC8
> .
@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:NP235012.RAvu6YtB1LENfdh5KHJgRm1LnDARFiYKergSlWJbKrsC8130_head
{
this:
np:hasAssertion
dgn-np:NP235012.RAvu6YtB1LENfdh5KHJgRm1LnDARFiYKergSlWJbKrsC8130_assertion
;
np:hasProvenance
dgn-np:NP235012.RAvu6YtB1LENfdh5KHJgRm1LnDARFiYKergSlWJbKrsC8130_provenance
;
np:hasPublicationInfo
dgn-np:NP235012.RAvu6YtB1LENfdh5KHJgRm1LnDARFiYKergSlWJbKrsC8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP235012.RAvu6YtB1LENfdh5KHJgRm1LnDARFiYKergSlWJbKrsC8130_assertion
a
np:Assertion
.
dgn-np:NP235012.RAvu6YtB1LENfdh5KHJgRm1LnDARFiYKergSlWJbKrsC8130_provenance
a
np:Provenance
.
dgn-np:NP235012.RAvu6YtB1LENfdh5KHJgRm1LnDARFiYKergSlWJbKrsC8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP235012.RAvu6YtB1LENfdh5KHJgRm1LnDARFiYKergSlWJbKrsC8130_assertion
{
miriam-gene:59271
a
ncit:C16612
.
lld:C1959635
a
ncit:C7057
.
dgn-gda:DGN51e8d792b2458bbfa574f94333e82179
sio:SIO_000628
miriam-gene:59271
,
lld:C1959635
;
a
sio:SIO_001121
.
}
dgn-np:NP235012.RAvu6YtB1LENfdh5KHJgRm1LnDARFiYKergSlWJbKrsC8130_provenance
{
dgn-np:NP235012.RAvu6YtB1LENfdh5KHJgRm1LnDARFiYKergSlWJbKrsC8130_assertion
dcterms:description
"[The human parvovirus B19 (B19) is etiologically related to human diseases, including erythema infectiosum and aplastic crisis, but it has not yet been considered to be involved in the development of ALL.]. 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:14966833
;
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:NP235012.RAvu6YtB1LENfdh5KHJgRm1LnDARFiYKergSlWJbKrsC8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:12+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" .
}