@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP892518.RATQ8rsMRQje2218Xn8fGA4dOhSfPBV5b5kvEUvj44NMA
> .
@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:NP892518.RATQ8rsMRQje2218Xn8fGA4dOhSfPBV5b5kvEUvj44NMA130_head
{
this:
np:hasAssertion
dgn-np:NP892518.RATQ8rsMRQje2218Xn8fGA4dOhSfPBV5b5kvEUvj44NMA130_assertion
;
np:hasProvenance
dgn-np:NP892518.RATQ8rsMRQje2218Xn8fGA4dOhSfPBV5b5kvEUvj44NMA130_provenance
;
np:hasPublicationInfo
dgn-np:NP892518.RATQ8rsMRQje2218Xn8fGA4dOhSfPBV5b5kvEUvj44NMA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP892518.RATQ8rsMRQje2218Xn8fGA4dOhSfPBV5b5kvEUvj44NMA130_assertion
a
np:Assertion
.
dgn-np:NP892518.RATQ8rsMRQje2218Xn8fGA4dOhSfPBV5b5kvEUvj44NMA130_provenance
a
np:Provenance
.
dgn-np:NP892518.RATQ8rsMRQje2218Xn8fGA4dOhSfPBV5b5kvEUvj44NMA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP892518.RATQ8rsMRQje2218Xn8fGA4dOhSfPBV5b5kvEUvj44NMA130_assertion
{
miriam-gene:30811
a
ncit:C16612
.
lld:C0854268
a
ncit:C7057
.
dgn-gda:DGN910b99d251289eff563e8641e0ba0aa1
sio:SIO_000628
miriam-gene:30811
,
lld:C0854268
;
a
sio:SIO_001121
.
}
dgn-np:NP892518.RATQ8rsMRQje2218Xn8fGA4dOhSfPBV5b5kvEUvj44NMA130_provenance
{
dgn-np:NP892518.RATQ8rsMRQje2218Xn8fGA4dOhSfPBV5b5kvEUvj44NMA130_assertion
dcterms:description
"[While human parvovirus B19 is associated with fetal damage and chronic suppression of bone marrow in patients with leukemia, much less is known of the genomic characteristics of B19 isolated from damaged human fetuses and leukemia patients.]. 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:8492104
;
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:NP892518.RATQ8rsMRQje2218Xn8fGA4dOhSfPBV5b5kvEUvj44NMA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:08+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" .
}