@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP331676.RAbr3oXIXyoITDa4yWqclvSuF4gvHeC71DINhhNbM7Q2E
> .
@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:NP331676.RAbr3oXIXyoITDa4yWqclvSuF4gvHeC71DINhhNbM7Q2E130_head
{
this:
np:hasAssertion
dgn-np:NP331676.RAbr3oXIXyoITDa4yWqclvSuF4gvHeC71DINhhNbM7Q2E130_assertion
;
np:hasProvenance
dgn-np:NP331676.RAbr3oXIXyoITDa4yWqclvSuF4gvHeC71DINhhNbM7Q2E130_provenance
;
np:hasPublicationInfo
dgn-np:NP331676.RAbr3oXIXyoITDa4yWqclvSuF4gvHeC71DINhhNbM7Q2E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP331676.RAbr3oXIXyoITDa4yWqclvSuF4gvHeC71DINhhNbM7Q2E130_assertion
a
np:Assertion
.
dgn-np:NP331676.RAbr3oXIXyoITDa4yWqclvSuF4gvHeC71DINhhNbM7Q2E130_provenance
a
np:Provenance
.
dgn-np:NP331676.RAbr3oXIXyoITDa4yWqclvSuF4gvHeC71DINhhNbM7Q2E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP331676.RAbr3oXIXyoITDa4yWqclvSuF4gvHeC71DINhhNbM7Q2E130_assertion
{
miriam-gene:4314
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN0542d1c4ec0cf8fd1ffb80ce48f77ae2
sio:SIO_000628
miriam-gene:4314
,
lld:C0003873
;
a
sio:SIO_001121
.
}
dgn-np:NP331676.RAbr3oXIXyoITDa4yWqclvSuF4gvHeC71DINhhNbM7Q2E130_provenance
{
dgn-np:NP331676.RAbr3oXIXyoITDa4yWqclvSuF4gvHeC71DINhhNbM7Q2E130_assertion
dcterms:description
"[In this study, we investigated the relationship between plasma homocysteine levels and single nucleotide polymorphism (SNP) of the gene coding for methylenetetrahydrofolate reductase (MTHFR), an enzyme involved in the biosynthesis of homocysteine, and the correlation between the plasma homocysteine levels and generally used inflammatory markers (C-reactive protein, erythrocyte sedimentation rate and matrix metalloproteinase-3) in 96 Japanese patients with RA.]. 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:19283524
;
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:NP331676.RAbr3oXIXyoITDa4yWqclvSuF4gvHeC71DINhhNbM7Q2E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:15+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" .
}