@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP756569.RAas_8l9g0fyX2w_8jVWylUgsi9Ek4Dz5iXmOQ1sd1q7o
> .
@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:NP756569.RAas_8l9g0fyX2w_8jVWylUgsi9Ek4Dz5iXmOQ1sd1q7o130_head
{
this:
np:hasAssertion
dgn-np:NP756569.RAas_8l9g0fyX2w_8jVWylUgsi9Ek4Dz5iXmOQ1sd1q7o130_assertion
;
np:hasProvenance
dgn-np:NP756569.RAas_8l9g0fyX2w_8jVWylUgsi9Ek4Dz5iXmOQ1sd1q7o130_provenance
;
np:hasPublicationInfo
dgn-np:NP756569.RAas_8l9g0fyX2w_8jVWylUgsi9Ek4Dz5iXmOQ1sd1q7o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP756569.RAas_8l9g0fyX2w_8jVWylUgsi9Ek4Dz5iXmOQ1sd1q7o130_assertion
a
np:Assertion
.
dgn-np:NP756569.RAas_8l9g0fyX2w_8jVWylUgsi9Ek4Dz5iXmOQ1sd1q7o130_provenance
a
np:Provenance
.
dgn-np:NP756569.RAas_8l9g0fyX2w_8jVWylUgsi9Ek4Dz5iXmOQ1sd1q7o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP756569.RAas_8l9g0fyX2w_8jVWylUgsi9Ek4Dz5iXmOQ1sd1q7o130_assertion
{
miriam-gene:391051
a
ncit:C16612
.
lld:C1332977
a
ncit:C7057
.
dgn-gda:DGNade7452e2111e17e86429fb95a85776f
sio:SIO_000628
miriam-gene:391051
,
lld:C1332977
;
a
sio:SIO_001121
.
}
dgn-np:NP756569.RAas_8l9g0fyX2w_8jVWylUgsi9Ek4Dz5iXmOQ1sd1q7o130_provenance
{
dgn-np:NP756569.RAas_8l9g0fyX2w_8jVWylUgsi9Ek4Dz5iXmOQ1sd1q7o130_assertion
dcterms:description
"[A most remarkable new development in the induction therapy of childhood leukemia and lymphoma in the United States is the use of urate oxidase for prevention of tumor lysis syndrome and the associated uric acid nephropathy.]. 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:12490758
;
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:NP756569.RAas_8l9g0fyX2w_8jVWylUgsi9Ek4Dz5iXmOQ1sd1q7o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:38+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" .
}