@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP926170.RAVWCZ1wu_vhS1DDA6AImuzn0rMcHF1M0e5oy1FHBmUXQ
> .
@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:NP926170.RAVWCZ1wu_vhS1DDA6AImuzn0rMcHF1M0e5oy1FHBmUXQ130_head
{
this:
np:hasAssertion
dgn-np:NP926170.RAVWCZ1wu_vhS1DDA6AImuzn0rMcHF1M0e5oy1FHBmUXQ130_assertion
;
np:hasProvenance
dgn-np:NP926170.RAVWCZ1wu_vhS1DDA6AImuzn0rMcHF1M0e5oy1FHBmUXQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP926170.RAVWCZ1wu_vhS1DDA6AImuzn0rMcHF1M0e5oy1FHBmUXQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP926170.RAVWCZ1wu_vhS1DDA6AImuzn0rMcHF1M0e5oy1FHBmUXQ130_assertion
a
np:Assertion
.
dgn-np:NP926170.RAVWCZ1wu_vhS1DDA6AImuzn0rMcHF1M0e5oy1FHBmUXQ130_provenance
a
np:Provenance
.
dgn-np:NP926170.RAVWCZ1wu_vhS1DDA6AImuzn0rMcHF1M0e5oy1FHBmUXQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP926170.RAVWCZ1wu_vhS1DDA6AImuzn0rMcHF1M0e5oy1FHBmUXQ130_assertion
{
miriam-gene:5744
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGNd07b558aef70497be2125f093b4fa8a7
sio:SIO_000628
miriam-gene:5744
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP926170.RAVWCZ1wu_vhS1DDA6AImuzn0rMcHF1M0e5oy1FHBmUXQ130_provenance
{
dgn-np:NP926170.RAVWCZ1wu_vhS1DDA6AImuzn0rMcHF1M0e5oy1FHBmUXQ130_assertion
dcterms:description
"[Fasting total plasma Hcy, folate, pyridoxal 5'-phosphate (PLP; active B6), B12, creatinine, glucose, total and HDL cholesterol levels, and presence of the ala to val MTHFR mutation were determined, and clinical CVD and CVD risk factor prevalence were ascertained.]. 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:8782850
;
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:NP926170.RAVWCZ1wu_vhS1DDA6AImuzn0rMcHF1M0e5oy1FHBmUXQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}