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http://rdf.disgenet.org/nanopublications.trig#NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_head
{
this:
np:hasAssertion
dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_assertion
;
np:hasProvenance
dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_provenance
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np:hasPublicationInfo
dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_assertion
a
np:Assertion
.
dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_provenance
a
np:Provenance
.
dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_assertion
{
miriam-gene:4709
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGN193f7e7fdc4eb2d42fb8cd1072039706
sio:SIO_000628
miriam-gene:4709
,
lld:C0011854
;
a
sio:SIO_001121
.
}
dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_provenance
{
dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_assertion
dcterms:description
"[The objectives of this study were: to determine plasma total homocysteine tHcy levels and the prevalence of hyperhomocysteinemia in children with type 1 diabetes, to determine correlates of plasma tHcy levels with nutritional factor such as serum folic acid and vitamin B12 levels, genetic factors as methylenetetrahydrofolate reductase MTHFR gene polymorphism (C677T and A1298C), to attempt to identify possible dependencies between tHcy and the degree of metabolic control, the duration of the disease and presence of complications, and also to determine the relationship between other coronary risk factors.]. 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:16401615
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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> , <
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> , <
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> ;
pav:createdBy
<
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> ;
pav:version
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