@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP654522.RAGeR1tvg1UrFZEV_npViIpoDDcDPtzLVUxKdgfYiKxnw
> .
@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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{
this:
np:hasAssertion
dgn-np:NP654522.RAGeR1tvg1UrFZEV_npViIpoDDcDPtzLVUxKdgfYiKxnw130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP654522.RAGeR1tvg1UrFZEV_npViIpoDDcDPtzLVUxKdgfYiKxnw130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP654522.RAGeR1tvg1UrFZEV_npViIpoDDcDPtzLVUxKdgfYiKxnw130_assertion
a
np:Assertion
.
dgn-np:NP654522.RAGeR1tvg1UrFZEV_npViIpoDDcDPtzLVUxKdgfYiKxnw130_provenance
a
np:Provenance
.
dgn-np:NP654522.RAGeR1tvg1UrFZEV_npViIpoDDcDPtzLVUxKdgfYiKxnw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP654522.RAGeR1tvg1UrFZEV_npViIpoDDcDPtzLVUxKdgfYiKxnw130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0085669
a
ncit:C7057
.
dgn-gda:DGN496aa85913a35796ba5896823d10619f
sio:SIO_000628
miriam-gene:2944
,
lld:C0085669
;
a
sio:SIO_001121
.
}
dgn-np:NP654522.RAGeR1tvg1UrFZEV_npViIpoDDcDPtzLVUxKdgfYiKxnw130_provenance
{
dgn-np:NP654522.RAGeR1tvg1UrFZEV_npViIpoDDcDPtzLVUxKdgfYiKxnw130_assertion
dcterms:description
"[Studying the relationship between polymorphisms of these genes and the outcome of our cases revealed the wild genotype of CYP2D6 significantly influenced the outcome of acute leukaemia particularly in AML cases, while GSTM1 null genotype was associated with bad prognosis among the ALL group.]. 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:17581325
;
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 .
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dgn-np:NP654522.RAGeR1tvg1UrFZEV_npViIpoDDcDPtzLVUxKdgfYiKxnw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:34+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
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> , <
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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pav:version
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