@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47500.RAdTHneNAsQF7UvcgPZ8QEWA-I7nDQOcClPvGXhpG2xxU
> .
@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:NP47500.RAdTHneNAsQF7UvcgPZ8QEWA-I7nDQOcClPvGXhpG2xxU130_head
{
this:
np:hasAssertion
dgn-np:NP47500.RAdTHneNAsQF7UvcgPZ8QEWA-I7nDQOcClPvGXhpG2xxU130_assertion
;
np:hasProvenance
dgn-np:NP47500.RAdTHneNAsQF7UvcgPZ8QEWA-I7nDQOcClPvGXhpG2xxU130_provenance
;
np:hasPublicationInfo
dgn-np:NP47500.RAdTHneNAsQF7UvcgPZ8QEWA-I7nDQOcClPvGXhpG2xxU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47500.RAdTHneNAsQF7UvcgPZ8QEWA-I7nDQOcClPvGXhpG2xxU130_assertion
a
np:Assertion
.
dgn-np:NP47500.RAdTHneNAsQF7UvcgPZ8QEWA-I7nDQOcClPvGXhpG2xxU130_provenance
a
np:Provenance
.
dgn-np:NP47500.RAdTHneNAsQF7UvcgPZ8QEWA-I7nDQOcClPvGXhpG2xxU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47500.RAdTHneNAsQF7UvcgPZ8QEWA-I7nDQOcClPvGXhpG2xxU130_assertion
{
miriam-gene:875
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN13c9bd7e4ef3f4a61bfedbf55c29427e
sio:SIO_000628
miriam-gene:875
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP47500.RAdTHneNAsQF7UvcgPZ8QEWA-I7nDQOcClPvGXhpG2xxU130_provenance
{
dgn-np:NP47500.RAdTHneNAsQF7UvcgPZ8QEWA-I7nDQOcClPvGXhpG2xxU130_assertion
dcterms:description
"[ This study provides additional evidence for a decreased CRC risk for subjects with the MTHFR 677T allele, particularly at high levels of folate and vitamin B6 intake. Our data also suggest that the relationships between CRC and the MTHFR A1298C and CBS 844ins68 polymorphisms warrant further study.]. 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:12020105
;
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:NP47500.RAdTHneNAsQF7UvcgPZ8QEWA-I7nDQOcClPvGXhpG2xxU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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
<
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" .
}