@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP84343.RARYvR2fQqfunykTYbdZiadTeFzGNNQ7kvOETpEfT3fY0
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP84343.RARYvR2fQqfunykTYbdZiadTeFzGNNQ7kvOETpEfT3fY0130_assertion
;
np:hasProvenance
dgn-np:NP84343.RARYvR2fQqfunykTYbdZiadTeFzGNNQ7kvOETpEfT3fY0130_provenance
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np:hasPublicationInfo
dgn-np:NP84343.RARYvR2fQqfunykTYbdZiadTeFzGNNQ7kvOETpEfT3fY0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP84343.RARYvR2fQqfunykTYbdZiadTeFzGNNQ7kvOETpEfT3fY0130_assertion
a
np:Assertion
.
dgn-np:NP84343.RARYvR2fQqfunykTYbdZiadTeFzGNNQ7kvOETpEfT3fY0130_provenance
a
np:Provenance
.
dgn-np:NP84343.RARYvR2fQqfunykTYbdZiadTeFzGNNQ7kvOETpEfT3fY0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP84343.RARYvR2fQqfunykTYbdZiadTeFzGNNQ7kvOETpEfT3fY0130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0079744
a
ncit:C7057
.
dgn-gda:DGNe6f8d31c41ce868142fdd265f60fc850
sio:SIO_000628
miriam-gene:4524
,
lld:C0079744
;
a
sio:SIO_001122
.
}
dgn-np:NP84343.RARYvR2fQqfunykTYbdZiadTeFzGNNQ7kvOETpEfT3fY0130_provenance
{
dgn-np:NP84343.RARYvR2fQqfunykTYbdZiadTeFzGNNQ7kvOETpEfT3fY0130_assertion
dcterms:description
"[We conducted a hospital-based case-control study including 160 DLBCL cases and 511 Saudi control samples analyzing the MTHFR C677T and A1298C functional polymorphisms by the restriction fragment length polymorphism method and their association with MGMT and FHIT genes promoter hypermethylation.]. 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:17712558
;
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:NP84343.RARYvR2fQqfunykTYbdZiadTeFzGNNQ7kvOETpEfT3fY0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:41+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
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"v2.1.0" .
}