@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP379634.RAz0Tot16QXRJvOYgEPeyYkbIT2TdpEcQcGliiTctiVpU
> .
@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:NP379634.RAz0Tot16QXRJvOYgEPeyYkbIT2TdpEcQcGliiTctiVpU130_head
{
this:
np:hasAssertion
dgn-np:NP379634.RAz0Tot16QXRJvOYgEPeyYkbIT2TdpEcQcGliiTctiVpU130_assertion
;
np:hasProvenance
dgn-np:NP379634.RAz0Tot16QXRJvOYgEPeyYkbIT2TdpEcQcGliiTctiVpU130_provenance
;
np:hasPublicationInfo
dgn-np:NP379634.RAz0Tot16QXRJvOYgEPeyYkbIT2TdpEcQcGliiTctiVpU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP379634.RAz0Tot16QXRJvOYgEPeyYkbIT2TdpEcQcGliiTctiVpU130_assertion
a
np:Assertion
.
dgn-np:NP379634.RAz0Tot16QXRJvOYgEPeyYkbIT2TdpEcQcGliiTctiVpU130_provenance
a
np:Provenance
.
dgn-np:NP379634.RAz0Tot16QXRJvOYgEPeyYkbIT2TdpEcQcGliiTctiVpU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP379634.RAz0Tot16QXRJvOYgEPeyYkbIT2TdpEcQcGliiTctiVpU130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN14594d39861769dca8c2cbb0951487aa
sio:SIO_000628
miriam-gene:4524
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP379634.RAz0Tot16QXRJvOYgEPeyYkbIT2TdpEcQcGliiTctiVpU130_provenance
{
dgn-np:NP379634.RAz0Tot16QXRJvOYgEPeyYkbIT2TdpEcQcGliiTctiVpU130_assertion
dcterms:description
"[In this case-control study, we examined C677T and A1298C (rs1801133 and rs1801131) polymorphism in the methylenetetrahydrofolate reductase (MTHFR) genes and their correlation with plasma levels of homocysteine (Hcy) in AD and VaD cases and evaluated the gene-gene interaction (epistasis) with IL-6-174 G/C (rs1800795).]. 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:22015309
;
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:NP379634.RAz0Tot16QXRJvOYgEPeyYkbIT2TdpEcQcGliiTctiVpU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:44+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" .
}