@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP255758.RAW31urgPb4yRFb6Nm9Rret3dSReoI3DNE1qLTCezW9FM
> .
@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:NP255758.RAW31urgPb4yRFb6Nm9Rret3dSReoI3DNE1qLTCezW9FM130_head
{
this:
np:hasAssertion
dgn-np:NP255758.RAW31urgPb4yRFb6Nm9Rret3dSReoI3DNE1qLTCezW9FM130_assertion
;
np:hasProvenance
dgn-np:NP255758.RAW31urgPb4yRFb6Nm9Rret3dSReoI3DNE1qLTCezW9FM130_provenance
;
np:hasPublicationInfo
dgn-np:NP255758.RAW31urgPb4yRFb6Nm9Rret3dSReoI3DNE1qLTCezW9FM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP255758.RAW31urgPb4yRFb6Nm9Rret3dSReoI3DNE1qLTCezW9FM130_assertion
a
np:Assertion
.
dgn-np:NP255758.RAW31urgPb4yRFb6Nm9Rret3dSReoI3DNE1qLTCezW9FM130_provenance
a
np:Provenance
.
dgn-np:NP255758.RAW31urgPb4yRFb6Nm9Rret3dSReoI3DNE1qLTCezW9FM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP255758.RAW31urgPb4yRFb6Nm9Rret3dSReoI3DNE1qLTCezW9FM130_assertion
{
miriam-gene:2122
a
ncit:C16612
.
lld:C0023470
a
ncit:C7057
.
dgn-gda:DGNaaacb7a364bdb72d8cc340ece9436520
sio:SIO_000628
miriam-gene:2122
,
lld:C0023470
;
a
sio:SIO_001121
.
}
dgn-np:NP255758.RAW31urgPb4yRFb6Nm9Rret3dSReoI3DNE1qLTCezW9FM130_provenance
{
dgn-np:NP255758.RAW31urgPb4yRFb6Nm9Rret3dSReoI3DNE1qLTCezW9FM130_assertion
dcterms:description
"[Thus, it is likely that overexpression of the zinc finger protein lacking the PR domain (EVI1 and MEL1S) in the leukemia cells is one of the causative factors in the pathogenesis of myeloid leukemia.]. 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:12816872
;
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:NP255758.RAW31urgPb4yRFb6Nm9Rret3dSReoI3DNE1qLTCezW9FM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:23+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" .
}