@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP42859.RAtEe2bC_ygaihFUezu4-UO5EvjxKJ8uoxGFqa18DcWSE
> .
@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 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:NP42859.RAtEe2bC_ygaihFUezu4-UO5EvjxKJ8uoxGFqa18DcWSE130_head
{
this:
np:hasAssertion
dgn-np:NP42859.RAtEe2bC_ygaihFUezu4-UO5EvjxKJ8uoxGFqa18DcWSE130_assertion
;
np:hasProvenance
dgn-np:NP42859.RAtEe2bC_ygaihFUezu4-UO5EvjxKJ8uoxGFqa18DcWSE130_provenance
;
np:hasPublicationInfo
dgn-np:NP42859.RAtEe2bC_ygaihFUezu4-UO5EvjxKJ8uoxGFqa18DcWSE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP42859.RAtEe2bC_ygaihFUezu4-UO5EvjxKJ8uoxGFqa18DcWSE130_assertion
a
np:Assertion
.
dgn-np:NP42859.RAtEe2bC_ygaihFUezu4-UO5EvjxKJ8uoxGFqa18DcWSE130_provenance
a
np:Provenance
.
dgn-np:NP42859.RAtEe2bC_ygaihFUezu4-UO5EvjxKJ8uoxGFqa18DcWSE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP42859.RAtEe2bC_ygaihFUezu4-UO5EvjxKJ8uoxGFqa18DcWSE130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0024305
a
ncit:C7057
.
dgn-gda:DGNc6744ada42e32d512f593bdd6fd81553
sio:SIO_000628
miriam-gene:2952
,
lld:C0024305
;
a
sio:SIO_001122
.
}
dgn-np:NP42859.RAtEe2bC_ygaihFUezu4-UO5EvjxKJ8uoxGFqa18DcWSE130_provenance
{
dgn-np:NP42859.RAtEe2bC_ygaihFUezu4-UO5EvjxKJ8uoxGFqa18DcWSE130_assertion
dct:description
"[We conclude that the two polymorphisms, GSTT1 null and PON1 BB, are common genetic traits that pose low individual risk but may be important determinants of overall population NHL risk, particularly among groups exposed to NHL-related carcinogens.]. 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:12139735
;
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:NP42859.RAtEe2bC_ygaihFUezu4-UO5EvjxKJ8uoxGFqa18DcWSE130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:19+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}