@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU
> .
@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:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_head
{
this:
np:hasAssertion
dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_assertion
;
np:hasProvenance
dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_provenance
;
np:hasPublicationInfo
dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_assertion
a
np:Assertion
.
dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_provenance
a
np:Provenance
.
dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_assertion
{
miriam-gene:7490
a
ncit:C16612
.
lld:C0002893
a
ncit:C7057
.
dgn-gda:DGNb9e8a2718d39e15a9b797b96e8cf70f5
sio:SIO_000628
miriam-gene:7490
,
lld:C0002893
;
a
sio:SIO_001121
.
}
dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_provenance
{
dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_assertion
dcterms:description
"[An increase of all three WT1 messages in high-grade MDS and acute leukemia was observed as compared with the normal control, whereas there was no significant difference in WT1 message between AA and RA, suggesting that WT1 message is not a good tool to discriminate AA and RA.]. 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:17803653
;
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:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}