@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP536372.RAf9h7MdSHJRLE6ky8JrHVt5SalVGH2oyC9z41ZtH9ZbU
> .
@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:NP536372.RAf9h7MdSHJRLE6ky8JrHVt5SalVGH2oyC9z41ZtH9ZbU130_head
{
this:
np:hasAssertion
dgn-np:NP536372.RAf9h7MdSHJRLE6ky8JrHVt5SalVGH2oyC9z41ZtH9ZbU130_assertion
;
np:hasProvenance
dgn-np:NP536372.RAf9h7MdSHJRLE6ky8JrHVt5SalVGH2oyC9z41ZtH9ZbU130_provenance
;
np:hasPublicationInfo
dgn-np:NP536372.RAf9h7MdSHJRLE6ky8JrHVt5SalVGH2oyC9z41ZtH9ZbU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP536372.RAf9h7MdSHJRLE6ky8JrHVt5SalVGH2oyC9z41ZtH9ZbU130_assertion
a
np:Assertion
.
dgn-np:NP536372.RAf9h7MdSHJRLE6ky8JrHVt5SalVGH2oyC9z41ZtH9ZbU130_provenance
a
np:Provenance
.
dgn-np:NP536372.RAf9h7MdSHJRLE6ky8JrHVt5SalVGH2oyC9z41ZtH9ZbU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP536372.RAf9h7MdSHJRLE6ky8JrHVt5SalVGH2oyC9z41ZtH9ZbU130_assertion
{
miriam-gene:4255
a
ncit:C16612
.
lld:C0598766
a
ncit:C7057
.
dgn-gda:DGNedbb5e8578e4a04c4fadfcafedf6cd96
sio:SIO_000628
miriam-gene:4255
,
lld:C0598766
;
a
sio:SIO_001121
.
}
dgn-np:NP536372.RAf9h7MdSHJRLE6ky8JrHVt5SalVGH2oyC9z41ZtH9ZbU130_provenance
{
dgn-np:NP536372.RAf9h7MdSHJRLE6ky8JrHVt5SalVGH2oyC9z41ZtH9ZbU130_assertion
dcterms:description
"[The association of genetic variants in MGMT with increased risk of NHL suggests that alkyl adducts may contribute to lymphomagenesis, and points to environmental and endogenous alkylating agents as possible risk factors for NHL.]. 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:17666372
;
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:NP536372.RAf9h7MdSHJRLE6ky8JrHVt5SalVGH2oyC9z41ZtH9ZbU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:23+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" .
}