@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP505770.RAgldlrhn2QbgkTEhy5FZwczpLCgfAt18lJmZMtO8_uvE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP505770.RAgldlrhn2QbgkTEhy5FZwczpLCgfAt18lJmZMtO8_uvE130_head
{
this:
np:hasAssertion
dgn-np:NP505770.RAgldlrhn2QbgkTEhy5FZwczpLCgfAt18lJmZMtO8_uvE130_assertion
;
np:hasProvenance
dgn-np:NP505770.RAgldlrhn2QbgkTEhy5FZwczpLCgfAt18lJmZMtO8_uvE130_provenance
;
np:hasPublicationInfo
dgn-np:NP505770.RAgldlrhn2QbgkTEhy5FZwczpLCgfAt18lJmZMtO8_uvE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP505770.RAgldlrhn2QbgkTEhy5FZwczpLCgfAt18lJmZMtO8_uvE130_assertion
a
np:Assertion
.
dgn-np:NP505770.RAgldlrhn2QbgkTEhy5FZwczpLCgfAt18lJmZMtO8_uvE130_provenance
a
np:Provenance
.
dgn-np:NP505770.RAgldlrhn2QbgkTEhy5FZwczpLCgfAt18lJmZMtO8_uvE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP505770.RAgldlrhn2QbgkTEhy5FZwczpLCgfAt18lJmZMtO8_uvE130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGN454df281f57785491d967c547104e242
sio:SIO_000628
miriam-gene:4524
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP505770.RAgldlrhn2QbgkTEhy5FZwczpLCgfAt18lJmZMtO8_uvE130_provenance
{
dgn-np:NP505770.RAgldlrhn2QbgkTEhy5FZwczpLCgfAt18lJmZMtO8_uvE130_assertion
dcterms:description
"[Common polymorphisms at the MTHFR nucleotides position 677 (C-T) and a 28-bp tandem repeat polymorphism (2R or 3R) in the TS promoter enhancer region (TSER) have been reported to be functional and are supposed to disturb the normal DNA methylation and synthesis leading to carcinogenesis.]. 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:16045580
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP505770.RAgldlrhn2QbgkTEhy5FZwczpLCgfAt18lJmZMtO8_uvE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:34+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}