@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP769903.RAbMlX3iA63gDX_0tAk0MHEuA72xkHlpHw5uAGKGi5zSM
> .
@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:NP769903.RAbMlX3iA63gDX_0tAk0MHEuA72xkHlpHw5uAGKGi5zSM130_head
{
this:
np:hasAssertion
dgn-np:NP769903.RAbMlX3iA63gDX_0tAk0MHEuA72xkHlpHw5uAGKGi5zSM130_assertion
;
np:hasProvenance
dgn-np:NP769903.RAbMlX3iA63gDX_0tAk0MHEuA72xkHlpHw5uAGKGi5zSM130_provenance
;
np:hasPublicationInfo
dgn-np:NP769903.RAbMlX3iA63gDX_0tAk0MHEuA72xkHlpHw5uAGKGi5zSM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP769903.RAbMlX3iA63gDX_0tAk0MHEuA72xkHlpHw5uAGKGi5zSM130_assertion
a
np:Assertion
.
dgn-np:NP769903.RAbMlX3iA63gDX_0tAk0MHEuA72xkHlpHw5uAGKGi5zSM130_provenance
a
np:Provenance
.
dgn-np:NP769903.RAbMlX3iA63gDX_0tAk0MHEuA72xkHlpHw5uAGKGi5zSM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP769903.RAbMlX3iA63gDX_0tAk0MHEuA72xkHlpHw5uAGKGi5zSM130_assertion
{
miriam-gene:4552
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN487fea4c3da2210cac72315f7dd3f535
sio:SIO_000628
miriam-gene:4552
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP769903.RAbMlX3iA63gDX_0tAk0MHEuA72xkHlpHw5uAGKGi5zSM130_provenance
{
dgn-np:NP769903.RAbMlX3iA63gDX_0tAk0MHEuA72xkHlpHw5uAGKGi5zSM130_assertion
dcterms:description
"[In the present study, we have assessed the association of six polymorphisms and relative haplotypes in the MTHFR gene (rs1801133 and rs1801131) and in the MTRR gene (rs1801394, rs1532268, rs162036, and rs10380) with the risk for colorectal cancer in 666 patients and 1377 controls from the Czech Republic.]. 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:21211571
;
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:NP769903.RAbMlX3iA63gDX_0tAk0MHEuA72xkHlpHw5uAGKGi5zSM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:46+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" .
}