@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP594005.RAAjrlKzCphsR_BQVsWYQFn8i0IOMOtjC3zq6txpfXLIM
> .
@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:NP594005.RAAjrlKzCphsR_BQVsWYQFn8i0IOMOtjC3zq6txpfXLIM130_head
{
this:
np:hasAssertion
dgn-np:NP594005.RAAjrlKzCphsR_BQVsWYQFn8i0IOMOtjC3zq6txpfXLIM130_assertion
;
np:hasProvenance
dgn-np:NP594005.RAAjrlKzCphsR_BQVsWYQFn8i0IOMOtjC3zq6txpfXLIM130_provenance
;
np:hasPublicationInfo
dgn-np:NP594005.RAAjrlKzCphsR_BQVsWYQFn8i0IOMOtjC3zq6txpfXLIM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP594005.RAAjrlKzCphsR_BQVsWYQFn8i0IOMOtjC3zq6txpfXLIM130_assertion
a
np:Assertion
.
dgn-np:NP594005.RAAjrlKzCphsR_BQVsWYQFn8i0IOMOtjC3zq6txpfXLIM130_provenance
a
np:Provenance
.
dgn-np:NP594005.RAAjrlKzCphsR_BQVsWYQFn8i0IOMOtjC3zq6txpfXLIM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP594005.RAAjrlKzCphsR_BQVsWYQFn8i0IOMOtjC3zq6txpfXLIM130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNfc3f4c8bab57eefeed94b62fed4392d3
sio:SIO_000628
miriam-gene:2944
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP594005.RAAjrlKzCphsR_BQVsWYQFn8i0IOMOtjC3zq6txpfXLIM130_provenance
{
dgn-np:NP594005.RAAjrlKzCphsR_BQVsWYQFn8i0IOMOtjC3zq6txpfXLIM130_assertion
dcterms:description
"[If we further divide the AML group into patients in which the burden of DNA damage is increased, because of the deletion of the GSTM1 gene, the risk of development of AML is further increased (OR, 15.26; 95% CI, 1.83-127.27).]. 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:15102670
;
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:NP594005.RAAjrlKzCphsR_BQVsWYQFn8i0IOMOtjC3zq6txpfXLIM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:57+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" .
}