@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP561338.RA4rdvhP5TTFm1Y2wkMp8hn2ViEYrlHn1wJBjyhXfTgp8
> .
@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:NP561338.RA4rdvhP5TTFm1Y2wkMp8hn2ViEYrlHn1wJBjyhXfTgp8130_head
{
this:
np:hasAssertion
dgn-np:NP561338.RA4rdvhP5TTFm1Y2wkMp8hn2ViEYrlHn1wJBjyhXfTgp8130_assertion
;
np:hasProvenance
dgn-np:NP561338.RA4rdvhP5TTFm1Y2wkMp8hn2ViEYrlHn1wJBjyhXfTgp8130_provenance
;
np:hasPublicationInfo
dgn-np:NP561338.RA4rdvhP5TTFm1Y2wkMp8hn2ViEYrlHn1wJBjyhXfTgp8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP561338.RA4rdvhP5TTFm1Y2wkMp8hn2ViEYrlHn1wJBjyhXfTgp8130_assertion
a
np:Assertion
.
dgn-np:NP561338.RA4rdvhP5TTFm1Y2wkMp8hn2ViEYrlHn1wJBjyhXfTgp8130_provenance
a
np:Provenance
.
dgn-np:NP561338.RA4rdvhP5TTFm1Y2wkMp8hn2ViEYrlHn1wJBjyhXfTgp8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP561338.RA4rdvhP5TTFm1Y2wkMp8hn2ViEYrlHn1wJBjyhXfTgp8130_assertion
{
miriam-gene:2052
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNf296e93b817995200cdf862ceb559c84
sio:SIO_000628
miriam-gene:2052
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP561338.RA4rdvhP5TTFm1Y2wkMp8hn2ViEYrlHn1wJBjyhXfTgp8130_provenance
{
dgn-np:NP561338.RA4rdvhP5TTFm1Y2wkMp8hn2ViEYrlHn1wJBjyhXfTgp8130_assertion
dcterms:description
"[We tested the hypothesis that smoking as well as genetic polymorphisms in the microsomal epoxide hydrolase gene (HYL1), an enzyme involved in benzene metabolism, could be risk factors for AML with defined chromosomal abnormalities.]. 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: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:NP561338.RA4rdvhP5TTFm1Y2wkMp8hn2ViEYrlHn1wJBjyhXfTgp8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}