@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP431164.RAzGqb-50ioEkDdAZQQJwa8Y-otjuE0OYyWIs3iZFhf1o
> .
@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:NP431164.RAzGqb-50ioEkDdAZQQJwa8Y-otjuE0OYyWIs3iZFhf1o130_head
{
this:
np:hasAssertion
dgn-np:NP431164.RAzGqb-50ioEkDdAZQQJwa8Y-otjuE0OYyWIs3iZFhf1o130_assertion
;
np:hasProvenance
dgn-np:NP431164.RAzGqb-50ioEkDdAZQQJwa8Y-otjuE0OYyWIs3iZFhf1o130_provenance
;
np:hasPublicationInfo
dgn-np:NP431164.RAzGqb-50ioEkDdAZQQJwa8Y-otjuE0OYyWIs3iZFhf1o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP431164.RAzGqb-50ioEkDdAZQQJwa8Y-otjuE0OYyWIs3iZFhf1o130_assertion
a
np:Assertion
.
dgn-np:NP431164.RAzGqb-50ioEkDdAZQQJwa8Y-otjuE0OYyWIs3iZFhf1o130_provenance
a
np:Provenance
.
dgn-np:NP431164.RAzGqb-50ioEkDdAZQQJwa8Y-otjuE0OYyWIs3iZFhf1o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP431164.RAzGqb-50ioEkDdAZQQJwa8Y-otjuE0OYyWIs3iZFhf1o130_assertion
{
miriam-gene:978
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN8fac9104609505fcbbeed5d446847444
sio:SIO_000628
miriam-gene:978
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP431164.RAzGqb-50ioEkDdAZQQJwa8Y-otjuE0OYyWIs3iZFhf1o130_provenance
{
dgn-np:NP431164.RAzGqb-50ioEkDdAZQQJwa8Y-otjuE0OYyWIs3iZFhf1o130_assertion
dcterms:description
"[CDA A79C genotypes were determined in 457 children with acute myeloid leukaemia (AML) treated on the Children's Cancer Group (CCG) 2941 and 2961 protocols and analyzed the impact of CDA genotype on therapy outcomes.]. 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:19036079
;
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:NP431164.RAzGqb-50ioEkDdAZQQJwa8Y-otjuE0OYyWIs3iZFhf1o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+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" .
}