@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1381477.RAWPzAo5MWADU1qkGE7bSfODUP9n3XQHyRC6zGqYbWtfc
> .
@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:NP1381477.RAWPzAo5MWADU1qkGE7bSfODUP9n3XQHyRC6zGqYbWtfc130_head
{
this:
np:hasAssertion
dgn-np:NP1381477.RAWPzAo5MWADU1qkGE7bSfODUP9n3XQHyRC6zGqYbWtfc130_assertion
;
np:hasProvenance
dgn-np:NP1381477.RAWPzAo5MWADU1qkGE7bSfODUP9n3XQHyRC6zGqYbWtfc130_provenance
;
np:hasPublicationInfo
dgn-np:NP1381477.RAWPzAo5MWADU1qkGE7bSfODUP9n3XQHyRC6zGqYbWtfc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1381477.RAWPzAo5MWADU1qkGE7bSfODUP9n3XQHyRC6zGqYbWtfc130_assertion
a
np:Assertion
.
dgn-np:NP1381477.RAWPzAo5MWADU1qkGE7bSfODUP9n3XQHyRC6zGqYbWtfc130_provenance
a
np:Provenance
.
dgn-np:NP1381477.RAWPzAo5MWADU1qkGE7bSfODUP9n3XQHyRC6zGqYbWtfc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1381477.RAWPzAo5MWADU1qkGE7bSfODUP9n3XQHyRC6zGqYbWtfc130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGNd39792d8656e9c2feb8adae2f971b3be
sio:SIO_000628
miriam-gene:4524
,
lld:C0007222
;
a
sio:SIO_001122
.
}
dgn-np:NP1381477.RAWPzAo5MWADU1qkGE7bSfODUP9n3XQHyRC6zGqYbWtfc130_provenance
{
dgn-np:NP1381477.RAWPzAo5MWADU1qkGE7bSfODUP9n3XQHyRC6zGqYbWtfc130_assertion
dcterms:description
"[We conducted a cross-sectional analysis of demographics, the diet, tHcy level, presence of the C677T mutation in the methylenetetrahydrofolate reductase gene (a common genetic cause of elevated tHcy) in children, and the prevalence of parental CVD.]. 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:9323065
;
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:NP1381477.RAWPzAo5MWADU1qkGE7bSfODUP9n3XQHyRC6zGqYbWtfc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:12+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" .
}