@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To
> .
@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:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_head
{
this:
np:hasAssertion
dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_assertion
;
np:hasProvenance
dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_provenance
;
np:hasPublicationInfo
dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_assertion
a
np:Assertion
.
dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_provenance
a
np:Provenance
.
dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN088c35d4c50dbb91cc9879c243ba437d
sio:SIO_000628
miriam-gene:2944
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_provenance
{
dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_assertion
dcterms:description
"[The work studied possible association between genetic polymorphisms of CYP2D6, GSTM1, GSTT1and NQO1 and altered susceptibility to leukaemia, correlating these genetic polymorphisms with clinical prognostic data, response to therapy and relapse.]. 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 .
}
dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}