@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM
> .
@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:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_head
{
this:
np:hasAssertion
dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_assertion
;
np:hasProvenance
dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_provenance
;
np:hasPublicationInfo
dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_assertion
a
np:Assertion
.
dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_provenance
a
np:Provenance
.
dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0007102
a
ncit:C7057
.
dgn-gda:DGN191f7ecd740091fb6a8882af3e41ed8a
sio:SIO_000628
miriam-gene:4524
,
lld:C0007102
;
a
sio:SIO_001121
.
}
dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_provenance
{
dgn-np:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_assertion
dcterms:description
"[The hypothesis that these two pathways are the means by which folate modulates cancer risk is also supported by the epidemiological observation that a common polymorphism in the methylenetetrahydrofolate reductase (MTHFR; EC 1.5.1.20) gene differentially affects the relative risk of colon cancer depending on folate status, because MTHFR catalyzes the reaction that determines whether cellular folate is diverted into biological methylation or nucleotide synthesis.]. 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:12163703
;
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:NP339810.RAJRXX6El1S-C42xApw5wAOrfVIZCuo9rtyi3ToXh2_FM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:20+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" .
}