@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP252989.RAq8cQe307zlvLpprPatTBVxRmY9t6_rm9N1pLXOkRIvg
> .
@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:NP252989.RAq8cQe307zlvLpprPatTBVxRmY9t6_rm9N1pLXOkRIvg130_head
{
this:
np:hasAssertion
dgn-np:NP252989.RAq8cQe307zlvLpprPatTBVxRmY9t6_rm9N1pLXOkRIvg130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP252989.RAq8cQe307zlvLpprPatTBVxRmY9t6_rm9N1pLXOkRIvg130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP252989.RAq8cQe307zlvLpprPatTBVxRmY9t6_rm9N1pLXOkRIvg130_assertion
a
np:Assertion
.
dgn-np:NP252989.RAq8cQe307zlvLpprPatTBVxRmY9t6_rm9N1pLXOkRIvg130_provenance
a
np:Provenance
.
dgn-np:NP252989.RAq8cQe307zlvLpprPatTBVxRmY9t6_rm9N1pLXOkRIvg130_publicationInfo
a
np:PublicationInfo
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dgn-np:NP252989.RAq8cQe307zlvLpprPatTBVxRmY9t6_rm9N1pLXOkRIvg130_assertion
{
miriam-gene:7126
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN6fcc5c4145dbe4ac88b73edcd418ac10
sio:SIO_000628
miriam-gene:7126
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP252989.RAq8cQe307zlvLpprPatTBVxRmY9t6_rm9N1pLXOkRIvg130_provenance
{
dgn-np:NP252989.RAq8cQe307zlvLpprPatTBVxRmY9t6_rm9N1pLXOkRIvg130_assertion
dcterms:description
"[Using a cohort we have been studying in Linxian since 1985, we examined the relationship between incident ESCC and GCA cancers and three polymorphisms in two genes that code for enzymes that require folate and B(12) as cofactors: methionine synthase reductase (MTRR) A66G and methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C.]. 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:14652285
;
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:NP252989.RAq8cQe307zlvLpprPatTBVxRmY9t6_rm9N1pLXOkRIvg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:21+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
<
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> , <
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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}