@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP129999.RAOrpNkr5wXUEuSLEQQefeeS4QvqLiw98VrwxniGF2Fz8
> .
@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/v3.0.0/void/
> .
dgn-np:NP129999.RAOrpNkr5wXUEuSLEQQefeeS4QvqLiw98VrwxniGF2Fz8130_head
{
this:
np:hasAssertion
dgn-np:NP129999.RAOrpNkr5wXUEuSLEQQefeeS4QvqLiw98VrwxniGF2Fz8130_assertion
;
np:hasProvenance
dgn-np:NP129999.RAOrpNkr5wXUEuSLEQQefeeS4QvqLiw98VrwxniGF2Fz8130_provenance
;
np:hasPublicationInfo
dgn-np:NP129999.RAOrpNkr5wXUEuSLEQQefeeS4QvqLiw98VrwxniGF2Fz8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP129999.RAOrpNkr5wXUEuSLEQQefeeS4QvqLiw98VrwxniGF2Fz8130_assertion
a
np:Assertion
.
dgn-np:NP129999.RAOrpNkr5wXUEuSLEQQefeeS4QvqLiw98VrwxniGF2Fz8130_provenance
a
np:Provenance
.
dgn-np:NP129999.RAOrpNkr5wXUEuSLEQQefeeS4QvqLiw98VrwxniGF2Fz8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP129999.RAOrpNkr5wXUEuSLEQQefeeS4QvqLiw98VrwxniGF2Fz8130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C2919828
a
ncit:C7057
.
dgn-gda:DGN8c8e78ddf0d1b8f25464e64188163725
sio:SIO_000628
miriam-gene:4524
,
lld:C2919828
;
a
sio:SIO_001122
.
}
dgn-np:NP129999.RAOrpNkr5wXUEuSLEQQefeeS4QvqLiw98VrwxniGF2Fz8130_provenance
{
dgn-np:NP129999.RAOrpNkr5wXUEuSLEQQefeeS4QvqLiw98VrwxniGF2Fz8130_assertion
dcterms:description
"[Genetic polymorphism of MTHFR G1793A was strongly associated with UC. HHcy, folate deficiency and low vitamin B12 concentration were common phenomena in the UC patients of Hubei Han nationality. Our findings demonstrate that the genes related to Hcy metab]. 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:20979787
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP129999.RAOrpNkr5wXUEuSLEQQefeeS4QvqLiw98VrwxniGF2Fz8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:53+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}