@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8
> .
@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:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_head
{
this:
np:hasAssertion
dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_assertion
;
np:hasProvenance
dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_provenance
;
np:hasPublicationInfo
dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_assertion
a
np:Assertion
.
dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_provenance
a
np:Provenance
.
dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_assertion
{
miriam-gene:6948
a
ncit:C16612
.
lld:C0017154
a
ncit:C7057
.
dgn-gda:DGN0a3d9a4e10b2e273b097f3d73d0120ca
sio:SIO_000628
miriam-gene:6948
,
lld:C0017154
;
a
sio:SIO_001122
.
}
dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_provenance
{
dgn-np:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_assertion
dcterms:description
"[A genetic variant of TCN2 (rs9606756) related to lower vitamin B12 levels was more frequent in pernicious anaemia patients compared to controls, showing the plausibility of genetic factors determining the possible clinical manifestation of autoimmune gastritis.]. 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:25681243
;
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:NP1263593.RAi93ZQwuH8NoQxl3fxqT0hnI6gST2UVEu-NME1Xf3qE8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:19+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" .
}