@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP515084.RAQiluuNCtZRZrHaObQEk9ERn8Jm1nUN4vre3jEIlOmpg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP515084.RAQiluuNCtZRZrHaObQEk9ERn8Jm1nUN4vre3jEIlOmpg130_head
{
this:
np:hasAssertion
dgn-np:NP515084.RAQiluuNCtZRZrHaObQEk9ERn8Jm1nUN4vre3jEIlOmpg130_assertion
;
np:hasProvenance
dgn-np:NP515084.RAQiluuNCtZRZrHaObQEk9ERn8Jm1nUN4vre3jEIlOmpg130_provenance
;
np:hasPublicationInfo
dgn-np:NP515084.RAQiluuNCtZRZrHaObQEk9ERn8Jm1nUN4vre3jEIlOmpg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP515084.RAQiluuNCtZRZrHaObQEk9ERn8Jm1nUN4vre3jEIlOmpg130_assertion
a
np:Assertion
.
dgn-np:NP515084.RAQiluuNCtZRZrHaObQEk9ERn8Jm1nUN4vre3jEIlOmpg130_provenance
a
np:Provenance
.
dgn-np:NP515084.RAQiluuNCtZRZrHaObQEk9ERn8Jm1nUN4vre3jEIlOmpg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP515084.RAQiluuNCtZRZrHaObQEk9ERn8Jm1nUN4vre3jEIlOmpg130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0016412
a
ncit:C7057
.
dgn-gda:DGNe6f5103847fe76d796c4aaae108b3347
sio:SIO_000628
miriam-gene:4524
,
lld:C0016412
;
a
sio:SIO_001122
.
}
dgn-np:NP515084.RAQiluuNCtZRZrHaObQEk9ERn8Jm1nUN4vre3jEIlOmpg130_provenance
{
dgn-np:NP515084.RAQiluuNCtZRZrHaObQEk9ERn8Jm1nUN4vre3jEIlOmpg130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP515084.RAQiluuNCtZRZrHaObQEk9ERn8Jm1nUN4vre3jEIlOmpg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:38+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}