@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP638633.RACtBUxQ-s2TMve1v2pRvqQONstHBOC9r0pTzt7C8Wmz4
> .
@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:NP638633.RACtBUxQ-s2TMve1v2pRvqQONstHBOC9r0pTzt7C8Wmz4130_head
{
this:
np:hasAssertion
dgn-np:NP638633.RACtBUxQ-s2TMve1v2pRvqQONstHBOC9r0pTzt7C8Wmz4130_assertion
;
np:hasProvenance
dgn-np:NP638633.RACtBUxQ-s2TMve1v2pRvqQONstHBOC9r0pTzt7C8Wmz4130_provenance
;
np:hasPublicationInfo
dgn-np:NP638633.RACtBUxQ-s2TMve1v2pRvqQONstHBOC9r0pTzt7C8Wmz4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP638633.RACtBUxQ-s2TMve1v2pRvqQONstHBOC9r0pTzt7C8Wmz4130_assertion
a
np:Assertion
.
dgn-np:NP638633.RACtBUxQ-s2TMve1v2pRvqQONstHBOC9r0pTzt7C8Wmz4130_provenance
a
np:Provenance
.
dgn-np:NP638633.RACtBUxQ-s2TMve1v2pRvqQONstHBOC9r0pTzt7C8Wmz4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP638633.RACtBUxQ-s2TMve1v2pRvqQONstHBOC9r0pTzt7C8Wmz4130_assertion
{
miriam-gene:7490
a
ncit:C16612
.
lld:C0220615
a
ncit:C7057
.
dgn-gda:DGN3d971419b5ea40ed36f2d3c6d9f7551a
sio:SIO_000628
miriam-gene:7490
,
lld:C0220615
;
a
sio:SIO_001121
.
}
dgn-np:NP638633.RACtBUxQ-s2TMve1v2pRvqQONstHBOC9r0pTzt7C8Wmz4130_provenance
{
dgn-np:NP638633.RACtBUxQ-s2TMve1v2pRvqQONstHBOC9r0pTzt7C8Wmz4130_assertion
dcterms:description
"[These results therefore suggest that WT1 gene expression can provide useful information for minimal residual disease detection in adult AML patients and that combined use of control genes can give more informative results.]. 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:23111196
;
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:NP638633.RACtBUxQ-s2TMve1v2pRvqQONstHBOC9r0pTzt7C8Wmz4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:25+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" .
}