@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP920295.RAhxvxTZz6nCFBSuW-GWAcoZvJY7KyFADiNxsDY9l9Y-Y
> .
@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:NP920295.RAhxvxTZz6nCFBSuW-GWAcoZvJY7KyFADiNxsDY9l9Y-Y130_head
{
this:
np:hasAssertion
dgn-np:NP920295.RAhxvxTZz6nCFBSuW-GWAcoZvJY7KyFADiNxsDY9l9Y-Y130_assertion
;
np:hasProvenance
dgn-np:NP920295.RAhxvxTZz6nCFBSuW-GWAcoZvJY7KyFADiNxsDY9l9Y-Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP920295.RAhxvxTZz6nCFBSuW-GWAcoZvJY7KyFADiNxsDY9l9Y-Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP920295.RAhxvxTZz6nCFBSuW-GWAcoZvJY7KyFADiNxsDY9l9Y-Y130_assertion
a
np:Assertion
.
dgn-np:NP920295.RAhxvxTZz6nCFBSuW-GWAcoZvJY7KyFADiNxsDY9l9Y-Y130_provenance
a
np:Provenance
.
dgn-np:NP920295.RAhxvxTZz6nCFBSuW-GWAcoZvJY7KyFADiNxsDY9l9Y-Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP920295.RAhxvxTZz6nCFBSuW-GWAcoZvJY7KyFADiNxsDY9l9Y-Y130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0042847
a
ncit:C7057
.
dgn-gda:DGNe2967b6f67b64c2c1a4e53af50f5560c
sio:SIO_000628
miriam-gene:4524
,
lld:C0042847
;
a
sio:SIO_001122
.
}
dgn-np:NP920295.RAhxvxTZz6nCFBSuW-GWAcoZvJY7KyFADiNxsDY9l9Y-Y130_provenance
{
dgn-np:NP920295.RAhxvxTZz6nCFBSuW-GWAcoZvJY7KyFADiNxsDY9l9Y-Y130_assertion
dcterms:description
"[One of the plausible reasons for susceptibility of individuals with MTHFR C677T in the studied population to various disorders is the high frequency of hyperhomocysteinemia and vitamin B12 deficiency in the 'healthy population'.]. 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:21878957
;
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:NP920295.RAhxvxTZz6nCFBSuW-GWAcoZvJY7KyFADiNxsDY9l9Y-Y130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:41+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" .
}