@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP235065.RAwoUJGV0TTTVQoQ9ZNe41S6_tH8pTzOe6OLxzy7c1zrE
> .
@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:NP235065.RAwoUJGV0TTTVQoQ9ZNe41S6_tH8pTzOe6OLxzy7c1zrE130_head
{
this:
np:hasAssertion
dgn-np:NP235065.RAwoUJGV0TTTVQoQ9ZNe41S6_tH8pTzOe6OLxzy7c1zrE130_assertion
;
np:hasProvenance
dgn-np:NP235065.RAwoUJGV0TTTVQoQ9ZNe41S6_tH8pTzOe6OLxzy7c1zrE130_provenance
;
np:hasPublicationInfo
dgn-np:NP235065.RAwoUJGV0TTTVQoQ9ZNe41S6_tH8pTzOe6OLxzy7c1zrE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP235065.RAwoUJGV0TTTVQoQ9ZNe41S6_tH8pTzOe6OLxzy7c1zrE130_assertion
a
np:Assertion
.
dgn-np:NP235065.RAwoUJGV0TTTVQoQ9ZNe41S6_tH8pTzOe6OLxzy7c1zrE130_provenance
a
np:Provenance
.
dgn-np:NP235065.RAwoUJGV0TTTVQoQ9ZNe41S6_tH8pTzOe6OLxzy7c1zrE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP235065.RAwoUJGV0TTTVQoQ9ZNe41S6_tH8pTzOe6OLxzy7c1zrE130_assertion
{
miriam-gene:2950
a
ncit:C16612
.
lld:C0085409
a
ncit:C7057
.
dgn-gda:DGNddc06ea1f39a9ed872d21a40a1ca020e
sio:SIO_000628
miriam-gene:2950
,
lld:C0085409
;
a
sio:SIO_001121
.
}
dgn-np:NP235065.RAwoUJGV0TTTVQoQ9ZNe41S6_tH8pTzOe6OLxzy7c1zrE130_provenance
{
dgn-np:NP235065.RAwoUJGV0TTTVQoQ9ZNe41S6_tH8pTzOe6OLxzy7c1zrE130_assertion
dcterms:description
"[In the selected population the urinary styrene metabolites mandelic (MA) and phenylglyoxylic (PGA) acids were quantified, sister chromatid exchanges (SCE) and micronuclei (MN) were assessed in peripheral lymphocytes and all the subjects were genotyped for GSTM1, GSTT1 (gene deletions), GSTP1 (codon 105 ile==>val), EPHX1 (codons 113 tyr==>his and 139 his==>arg) and CYP2E1 (DraI polymorphism in intron 6).]. 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:14751678
;
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:NP235065.RAwoUJGV0TTTVQoQ9ZNe41S6_tH8pTzOe6OLxzy7c1zrE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:12+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" .
}