@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ
> .
@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:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_head
{
this:
np:hasAssertion
dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_assertion
;
np:hasProvenance
dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_assertion
a
np:Assertion
.
dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_provenance
a
np:Provenance
.
dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_assertion
{
miriam-gene:30811
a
ncit:C16612
.
lld:C0018939
a
ncit:C7057
.
dgn-gda:DGN45f03fb52a4b418ca2de6ae9c1d9f33c
sio:SIO_000628
miriam-gene:30811
,
lld:C0018939
;
a
sio:SIO_001121
.
}
dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_provenance
{
dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_assertion
dcterms:description
"[We conclude that patients with hematological disease have higher seropositive rates for B19 than occur in normal controls and that study of occult parvovirus B19 infection is recommended in patients with hematological disease.]. 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:14556276
;
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:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:08+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" .
}