@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP317950.RA4yu45TRvk34ZwDE3G3qTGqeAExG9lDY21eqeMDXo7_Q
> .
@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:NP317950.RA4yu45TRvk34ZwDE3G3qTGqeAExG9lDY21eqeMDXo7_Q130_head
{
this:
np:hasAssertion
dgn-np:NP317950.RA4yu45TRvk34ZwDE3G3qTGqeAExG9lDY21eqeMDXo7_Q130_assertion
;
np:hasProvenance
dgn-np:NP317950.RA4yu45TRvk34ZwDE3G3qTGqeAExG9lDY21eqeMDXo7_Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP317950.RA4yu45TRvk34ZwDE3G3qTGqeAExG9lDY21eqeMDXo7_Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP317950.RA4yu45TRvk34ZwDE3G3qTGqeAExG9lDY21eqeMDXo7_Q130_assertion
a
np:Assertion
.
dgn-np:NP317950.RA4yu45TRvk34ZwDE3G3qTGqeAExG9lDY21eqeMDXo7_Q130_provenance
a
np:Provenance
.
dgn-np:NP317950.RA4yu45TRvk34ZwDE3G3qTGqeAExG9lDY21eqeMDXo7_Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP317950.RA4yu45TRvk34ZwDE3G3qTGqeAExG9lDY21eqeMDXo7_Q130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C2750737
a
ncit:C7057
.
dgn-gda:DGN6b0f612174f3352ab02ffde7d4b4731d
sio:SIO_000628
miriam-gene:2944
,
lld:C2750737
;
a
sio:SIO_001121
.
}
dgn-np:NP317950.RA4yu45TRvk34ZwDE3G3qTGqeAExG9lDY21eqeMDXo7_Q130_provenance
{
dgn-np:NP317950.RA4yu45TRvk34ZwDE3G3qTGqeAExG9lDY21eqeMDXo7_Q130_assertion
dcterms:description
"[Therefore, we investigated the presence of null genotypes for glutathione S-transferases M1 and T1 (GSTM1, GSTT1) and two genetic polymorphisms of microsomal epoxide hydrolase (mEPHX) in relation to the risk for chronic toxic encephalopathy (CTE) when exposed to solvents and smoking.]. 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:14992466
;
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:NP317950.RA4yu45TRvk34ZwDE3G3qTGqeAExG9lDY21eqeMDXo7_Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:04+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
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dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}