@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP435151.RAur-gZYK0q02JgPS0H4xX47Yl77anR708ejg5_Bt9WTo
> .
@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:NP435151.RAur-gZYK0q02JgPS0H4xX47Yl77anR708ejg5_Bt9WTo130_head
{
this:
np:hasAssertion
dgn-np:NP435151.RAur-gZYK0q02JgPS0H4xX47Yl77anR708ejg5_Bt9WTo130_assertion
;
np:hasProvenance
dgn-np:NP435151.RAur-gZYK0q02JgPS0H4xX47Yl77anR708ejg5_Bt9WTo130_provenance
;
np:hasPublicationInfo
dgn-np:NP435151.RAur-gZYK0q02JgPS0H4xX47Yl77anR708ejg5_Bt9WTo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP435151.RAur-gZYK0q02JgPS0H4xX47Yl77anR708ejg5_Bt9WTo130_assertion
a
np:Assertion
.
dgn-np:NP435151.RAur-gZYK0q02JgPS0H4xX47Yl77anR708ejg5_Bt9WTo130_provenance
a
np:Provenance
.
dgn-np:NP435151.RAur-gZYK0q02JgPS0H4xX47Yl77anR708ejg5_Bt9WTo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP435151.RAur-gZYK0q02JgPS0H4xX47Yl77anR708ejg5_Bt9WTo130_assertion
{
miriam-gene:4709
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN803bb86503b2b15288ff590bf2c5936d
sio:SIO_000628
miriam-gene:4709
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP435151.RAur-gZYK0q02JgPS0H4xX47Yl77anR708ejg5_Bt9WTo130_provenance
{
dgn-np:NP435151.RAur-gZYK0q02JgPS0H4xX47Yl77anR708ejg5_Bt9WTo130_assertion
dcterms:description
"[In this study, we have investigated whether DNA damage is related to the C677T variant in the MTHFR gene and to plasma levels of Hcy, B12, and folate in patients with CAD.]. 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:12522558
;
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:NP435151.RAur-gZYK0q02JgPS0H4xX47Yl77anR708ejg5_Bt9WTo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:17+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" .
}