@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP738373.RAq8KkJ1dJ7UU81s2a28A16Jc1UDGBwT2XGe0C83DkO5E
> .
@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#
> .
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{
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np:hasAssertion
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;
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP738373.RAq8KkJ1dJ7UU81s2a28A16Jc1UDGBwT2XGe0C83DkO5E130_provenance
a
np:Provenance
.
dgn-np:NP738373.RAq8KkJ1dJ7UU81s2a28A16Jc1UDGBwT2XGe0C83DkO5E130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:2056
a
ncit:C16612
.
lld:C1961102
a
ncit:C7057
.
dgn-gda:DGNcc4f4dc207c50855e94f8d2fd26d1302
sio:SIO_000628
miriam-gene:2056
,
lld:C1961102
;
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.
}
dgn-np:NP738373.RAq8KkJ1dJ7UU81s2a28A16Jc1UDGBwT2XGe0C83DkO5E130_provenance
{
dgn-np:NP738373.RAq8KkJ1dJ7UU81s2a28A16Jc1UDGBwT2XGe0C83DkO5E130_assertion
dcterms:description
"[We genotyped the EPO rS1617640 SNP in 189 patients with MDS, 257 with acute myeloid leukemia (AML), 106 with acute lymphoblastic leukemia, 97 with chronic lymphocytic leukemia, 353 with chronic myeloid leukemia, and 95 healthy controls.]. 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:21078205
;
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:NP738373.RAq8KkJ1dJ7UU81s2a28A16Jc1UDGBwT2XGe0C83DkO5E130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
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> ;
pav:createdBy
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> ;
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