@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP244362.RAChzrGqrNxCz6VQgzvCfSSyfNTG01u1tXDqCWS9NIi50
> .
@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:NP244362.RAChzrGqrNxCz6VQgzvCfSSyfNTG01u1tXDqCWS9NIi50130_head
{
this:
np:hasAssertion
dgn-np:NP244362.RAChzrGqrNxCz6VQgzvCfSSyfNTG01u1tXDqCWS9NIi50130_assertion
;
np:hasProvenance
dgn-np:NP244362.RAChzrGqrNxCz6VQgzvCfSSyfNTG01u1tXDqCWS9NIi50130_provenance
;
np:hasPublicationInfo
dgn-np:NP244362.RAChzrGqrNxCz6VQgzvCfSSyfNTG01u1tXDqCWS9NIi50130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP244362.RAChzrGqrNxCz6VQgzvCfSSyfNTG01u1tXDqCWS9NIi50130_assertion
a
np:Assertion
.
dgn-np:NP244362.RAChzrGqrNxCz6VQgzvCfSSyfNTG01u1tXDqCWS9NIi50130_provenance
a
np:Provenance
.
dgn-np:NP244362.RAChzrGqrNxCz6VQgzvCfSSyfNTG01u1tXDqCWS9NIi50130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP244362.RAChzrGqrNxCz6VQgzvCfSSyfNTG01u1tXDqCWS9NIi50130_assertion
{
miriam-gene:25824
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN4fa99c7969b2dbb3e4179646d2c0d08b
sio:SIO_000628
miriam-gene:25824
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP244362.RAChzrGqrNxCz6VQgzvCfSSyfNTG01u1tXDqCWS9NIi50130_provenance
{
dgn-np:NP244362.RAChzrGqrNxCz6VQgzvCfSSyfNTG01u1tXDqCWS9NIi50130_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:NP244362.RAChzrGqrNxCz6VQgzvCfSSyfNTG01u1tXDqCWS9NIi50130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:16+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" .
}