@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP600548.RA5Rxb8rMFhiGGHZaNQKm10rWdGQtclElJLvMUWylBF_U
> .
@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:NP600548.RA5Rxb8rMFhiGGHZaNQKm10rWdGQtclElJLvMUWylBF_U130_head
{
this:
np:hasAssertion
dgn-np:NP600548.RA5Rxb8rMFhiGGHZaNQKm10rWdGQtclElJLvMUWylBF_U130_assertion
;
np:hasProvenance
dgn-np:NP600548.RA5Rxb8rMFhiGGHZaNQKm10rWdGQtclElJLvMUWylBF_U130_provenance
;
np:hasPublicationInfo
dgn-np:NP600548.RA5Rxb8rMFhiGGHZaNQKm10rWdGQtclElJLvMUWylBF_U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP600548.RA5Rxb8rMFhiGGHZaNQKm10rWdGQtclElJLvMUWylBF_U130_assertion
a
np:Assertion
.
dgn-np:NP600548.RA5Rxb8rMFhiGGHZaNQKm10rWdGQtclElJLvMUWylBF_U130_provenance
a
np:Provenance
.
dgn-np:NP600548.RA5Rxb8rMFhiGGHZaNQKm10rWdGQtclElJLvMUWylBF_U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP600548.RA5Rxb8rMFhiGGHZaNQKm10rWdGQtclElJLvMUWylBF_U130_assertion
{
miriam-gene:6667
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN4f1cd0e2b8f5d361e5cc4943025c0864
sio:SIO_000628
miriam-gene:6667
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP600548.RA5Rxb8rMFhiGGHZaNQKm10rWdGQtclElJLvMUWylBF_U130_provenance
{
dgn-np:NP600548.RA5Rxb8rMFhiGGHZaNQKm10rWdGQtclElJLvMUWylBF_U130_assertion
dcterms:description
"[Most cases of acute myelocytic leukemia are homozygous for the allele with the SP1 binding site, suggesting this element plays an important role in regulating the MPO gene in myeloid leukemias.]. 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:8662930
;
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:NP600548.RA5Rxb8rMFhiGGHZaNQKm10rWdGQtclElJLvMUWylBF_U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:00+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" .
}