@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP521617.RAdPFoSLoFo4rLt6D6PW8TjKuXVuxyAtkdqncrA3c8p08
> .
@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:NP521617.RAdPFoSLoFo4rLt6D6PW8TjKuXVuxyAtkdqncrA3c8p08130_head
{
this:
np:hasAssertion
dgn-np:NP521617.RAdPFoSLoFo4rLt6D6PW8TjKuXVuxyAtkdqncrA3c8p08130_assertion
;
np:hasProvenance
dgn-np:NP521617.RAdPFoSLoFo4rLt6D6PW8TjKuXVuxyAtkdqncrA3c8p08130_provenance
;
np:hasPublicationInfo
dgn-np:NP521617.RAdPFoSLoFo4rLt6D6PW8TjKuXVuxyAtkdqncrA3c8p08130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP521617.RAdPFoSLoFo4rLt6D6PW8TjKuXVuxyAtkdqncrA3c8p08130_assertion
a
np:Assertion
.
dgn-np:NP521617.RAdPFoSLoFo4rLt6D6PW8TjKuXVuxyAtkdqncrA3c8p08130_provenance
a
np:Provenance
.
dgn-np:NP521617.RAdPFoSLoFo4rLt6D6PW8TjKuXVuxyAtkdqncrA3c8p08130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP521617.RAdPFoSLoFo4rLt6D6PW8TjKuXVuxyAtkdqncrA3c8p08130_assertion
{
miriam-gene:59271
a
ncit:C16612
.
lld:C0020305
a
ncit:C7057
.
dgn-gda:DGN309135a77c49f466e8982be65f4074c2
sio:SIO_000628
miriam-gene:59271
,
lld:C0020305
;
a
sio:SIO_001121
.
}
dgn-np:NP521617.RAdPFoSLoFo4rLt6D6PW8TjKuXVuxyAtkdqncrA3c8p08130_provenance
{
dgn-np:NP521617.RAdPFoSLoFo4rLt6D6PW8TjKuXVuxyAtkdqncrA3c8p08130_assertion
dcterms:description
"[Disease outcomes of bone marrow failure in patients with high turnover of red blood cells and immunocompromised conditions, and fetal hydrops in pregnant women are resulted from the targeting and destruction of specifically erythroid progenitors of the human bone marrow by B19V.]. 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:21698228
;
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:NP521617.RAdPFoSLoFo4rLt6D6PW8TjKuXVuxyAtkdqncrA3c8p08130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:10+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" .
}