@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP894905.RAXfeFOZbMDnRs3s6W8edW1kkXsic__Q55ZbezLcrDSn0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP894905.RAXfeFOZbMDnRs3s6W8edW1kkXsic__Q55ZbezLcrDSn0130_head
{
this:
np:hasAssertion
dgn-np:NP894905.RAXfeFOZbMDnRs3s6W8edW1kkXsic__Q55ZbezLcrDSn0130_assertion
;
np:hasProvenance
dgn-np:NP894905.RAXfeFOZbMDnRs3s6W8edW1kkXsic__Q55ZbezLcrDSn0130_provenance
;
np:hasPublicationInfo
dgn-np:NP894905.RAXfeFOZbMDnRs3s6W8edW1kkXsic__Q55ZbezLcrDSn0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP894905.RAXfeFOZbMDnRs3s6W8edW1kkXsic__Q55ZbezLcrDSn0130_assertion
a
np:Assertion
.
dgn-np:NP894905.RAXfeFOZbMDnRs3s6W8edW1kkXsic__Q55ZbezLcrDSn0130_provenance
a
np:Provenance
.
dgn-np:NP894905.RAXfeFOZbMDnRs3s6W8edW1kkXsic__Q55ZbezLcrDSn0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP894905.RAXfeFOZbMDnRs3s6W8edW1kkXsic__Q55ZbezLcrDSn0130_assertion
{
miriam-gene:1543
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN4a25a3e29337cedb8fe07ebaa599ce85
sio:SIO_000628
miriam-gene:1543
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP894905.RAXfeFOZbMDnRs3s6W8edW1kkXsic__Q55ZbezLcrDSn0130_provenance
{
dgn-np:NP894905.RAXfeFOZbMDnRs3s6W8edW1kkXsic__Q55ZbezLcrDSn0130_assertion
dcterms:description
"[Our study suggests that polymorphisms in CYP1A1 may contribute to the increased risk of ALL in Hispanic children due to both their impact on leukemia susceptibility and the increased prevalence of the at-risk alleles in the Hispanic population.]. 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:21586621
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP894905.RAXfeFOZbMDnRs3s6W8edW1kkXsic__Q55ZbezLcrDSn0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:30+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}