@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP45087.RAHUTPc8hpMnBmer3JYo0zMw1z6A7G9VXmM77FY-FU60c
> .
@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:NP45087.RAHUTPc8hpMnBmer3JYo0zMw1z6A7G9VXmM77FY-FU60c130_head
{
this:
np:hasAssertion
dgn-np:NP45087.RAHUTPc8hpMnBmer3JYo0zMw1z6A7G9VXmM77FY-FU60c130_assertion
;
np:hasProvenance
dgn-np:NP45087.RAHUTPc8hpMnBmer3JYo0zMw1z6A7G9VXmM77FY-FU60c130_provenance
;
np:hasPublicationInfo
dgn-np:NP45087.RAHUTPc8hpMnBmer3JYo0zMw1z6A7G9VXmM77FY-FU60c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP45087.RAHUTPc8hpMnBmer3JYo0zMw1z6A7G9VXmM77FY-FU60c130_assertion
a
np:Assertion
.
dgn-np:NP45087.RAHUTPc8hpMnBmer3JYo0zMw1z6A7G9VXmM77FY-FU60c130_provenance
a
np:Provenance
.
dgn-np:NP45087.RAHUTPc8hpMnBmer3JYo0zMw1z6A7G9VXmM77FY-FU60c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP45087.RAHUTPc8hpMnBmer3JYo0zMw1z6A7G9VXmM77FY-FU60c130_assertion
{
miriam-gene:2052
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN508bf985f1fa72910657a3393e3ab6d9
sio:SIO_000628
miriam-gene:2052
,
lld:C0023467
;
a
sio:SIO_001122
.
}
dgn-np:NP45087.RAHUTPc8hpMnBmer3JYo0zMw1z6A7G9VXmM77FY-FU60c130_provenance
{
dgn-np:NP45087.RAHUTPc8hpMnBmer3JYo0zMw1z6A7G9VXmM77FY-FU60c130_assertion
dcterms:description
"[This suggests that AML cases with defined chromosomal abnormalities could be related to specific carcinogen exposures and, furthermore, suggests that smoking and genetic polymorphisms in HYL1 could be risk factors for AML with -7/del(7q) or t(8;21).]. 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:11849215
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP45087.RAHUTPc8hpMnBmer3JYo0zMw1z6A7G9VXmM77FY-FU60c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}