@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP437784.RAlCEyaFnqaGVlfW28C9lHebJQzmgH1RwHOMhq1QNESmU
> .
@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:NP437784.RAlCEyaFnqaGVlfW28C9lHebJQzmgH1RwHOMhq1QNESmU130_head
{
this:
np:hasAssertion
dgn-np:NP437784.RAlCEyaFnqaGVlfW28C9lHebJQzmgH1RwHOMhq1QNESmU130_assertion
;
np:hasProvenance
dgn-np:NP437784.RAlCEyaFnqaGVlfW28C9lHebJQzmgH1RwHOMhq1QNESmU130_provenance
;
np:hasPublicationInfo
dgn-np:NP437784.RAlCEyaFnqaGVlfW28C9lHebJQzmgH1RwHOMhq1QNESmU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP437784.RAlCEyaFnqaGVlfW28C9lHebJQzmgH1RwHOMhq1QNESmU130_assertion
a
np:Assertion
.
dgn-np:NP437784.RAlCEyaFnqaGVlfW28C9lHebJQzmgH1RwHOMhq1QNESmU130_provenance
a
np:Provenance
.
dgn-np:NP437784.RAlCEyaFnqaGVlfW28C9lHebJQzmgH1RwHOMhq1QNESmU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP437784.RAlCEyaFnqaGVlfW28C9lHebJQzmgH1RwHOMhq1QNESmU130_assertion
{
miriam-gene:4548
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGN3896bc089c12145a93626977b612d0b6
sio:SIO_000628
miriam-gene:4548
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP437784.RAlCEyaFnqaGVlfW28C9lHebJQzmgH1RwHOMhq1QNESmU130_provenance
{
dgn-np:NP437784.RAlCEyaFnqaGVlfW28C9lHebJQzmgH1RwHOMhq1QNESmU130_assertion
dcterms:description
"[Functional polymorphisms in genes encoding one-carbon metabolism enzymes, such as methylenetetrahydrofolate reductase (MTHFR C677T and A1298C), methionine synthase (MTR A2756G), methionine synthase reductase (MTRR A66G) and thymidylate synthase (TS), influence folate metabolism and thus might impact on HNSCC risk.]. 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:17596206
;
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:NP437784.RAlCEyaFnqaGVlfW28C9lHebJQzmgH1RwHOMhq1QNESmU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:19+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" .
}