@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1289334.RAKbAPbjeEU6GMV4tDaOOF7VcNa_OpBaHPj5cJ_57DkOc
> .
@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:NP1289334.RAKbAPbjeEU6GMV4tDaOOF7VcNa_OpBaHPj5cJ_57DkOc130_head
{
this:
np:hasAssertion
dgn-np:NP1289334.RAKbAPbjeEU6GMV4tDaOOF7VcNa_OpBaHPj5cJ_57DkOc130_assertion
;
np:hasProvenance
dgn-np:NP1289334.RAKbAPbjeEU6GMV4tDaOOF7VcNa_OpBaHPj5cJ_57DkOc130_provenance
;
np:hasPublicationInfo
dgn-np:NP1289334.RAKbAPbjeEU6GMV4tDaOOF7VcNa_OpBaHPj5cJ_57DkOc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1289334.RAKbAPbjeEU6GMV4tDaOOF7VcNa_OpBaHPj5cJ_57DkOc130_assertion
a
np:Assertion
.
dgn-np:NP1289334.RAKbAPbjeEU6GMV4tDaOOF7VcNa_OpBaHPj5cJ_57DkOc130_provenance
a
np:Provenance
.
dgn-np:NP1289334.RAKbAPbjeEU6GMV4tDaOOF7VcNa_OpBaHPj5cJ_57DkOc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1289334.RAKbAPbjeEU6GMV4tDaOOF7VcNa_OpBaHPj5cJ_57DkOc130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0856169
a
ncit:C7057
.
dgn-gda:DGN8ad3c358218c5ec3c5d23176a6b50d11
sio:SIO_000628
miriam-gene:4524
,
lld:C0856169
;
a
sio:SIO_001121
.
}
dgn-np:NP1289334.RAKbAPbjeEU6GMV4tDaOOF7VcNa_OpBaHPj5cJ_57DkOc130_provenance
{
dgn-np:NP1289334.RAKbAPbjeEU6GMV4tDaOOF7VcNa_OpBaHPj5cJ_57DkOc130_assertion
dcterms:description
"[To confirm previous observations on the association of homozygosity for the TT MTHFR genotype with B12 deficiency and endothelial dysfunction, and to investigate whether patients with B12 deficiency should be tested for 677MTHFR genotype.]. 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:26137654
;
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:NP1289334.RAKbAPbjeEU6GMV4tDaOOF7VcNa_OpBaHPj5cJ_57DkOc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:30+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" .
}