@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP396647.RAmkAOnlARcal4byEzdOaHxmJWYzqBdVGChqfjSxkUmSQ
> .
@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:NP396647.RAmkAOnlARcal4byEzdOaHxmJWYzqBdVGChqfjSxkUmSQ130_head
{
this:
np:hasAssertion
dgn-np:NP396647.RAmkAOnlARcal4byEzdOaHxmJWYzqBdVGChqfjSxkUmSQ130_assertion
;
np:hasProvenance
dgn-np:NP396647.RAmkAOnlARcal4byEzdOaHxmJWYzqBdVGChqfjSxkUmSQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP396647.RAmkAOnlARcal4byEzdOaHxmJWYzqBdVGChqfjSxkUmSQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP396647.RAmkAOnlARcal4byEzdOaHxmJWYzqBdVGChqfjSxkUmSQ130_assertion
a
np:Assertion
.
dgn-np:NP396647.RAmkAOnlARcal4byEzdOaHxmJWYzqBdVGChqfjSxkUmSQ130_provenance
a
np:Provenance
.
dgn-np:NP396647.RAmkAOnlARcal4byEzdOaHxmJWYzqBdVGChqfjSxkUmSQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP396647.RAmkAOnlARcal4byEzdOaHxmJWYzqBdVGChqfjSxkUmSQ130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0016412
a
ncit:C7057
.
dgn-gda:DGNc9964ccc0b27f3be67f1e189f94862b4
sio:SIO_000628
miriam-gene:4524
,
lld:C0016412
;
a
sio:SIO_001121
.
}
dgn-np:NP396647.RAmkAOnlARcal4byEzdOaHxmJWYzqBdVGChqfjSxkUmSQ130_provenance
{
dgn-np:NP396647.RAmkAOnlARcal4byEzdOaHxmJWYzqBdVGChqfjSxkUmSQ130_assertion
dcterms:description
"[The C677T mutation of the methylenetetrahydrofolate reductase gene may induce hyperhomocysteinemia and could slightly increase the risk of arterial or venous thrombosis and pregnancy loss in individuals with folic acid deficiency.]. 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:16185908
;
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:NP396647.RAmkAOnlARcal4byEzdOaHxmJWYzqBdVGChqfjSxkUmSQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:56+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" .
}