@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP311593.RAFSbNjT4Bdih4nAUhIOyc263IIzFyEI6ZTF1E8womFWg
> .
@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:NP311593.RAFSbNjT4Bdih4nAUhIOyc263IIzFyEI6ZTF1E8womFWg130_head
{
this:
np:hasAssertion
dgn-np:NP311593.RAFSbNjT4Bdih4nAUhIOyc263IIzFyEI6ZTF1E8womFWg130_assertion
;
np:hasProvenance
dgn-np:NP311593.RAFSbNjT4Bdih4nAUhIOyc263IIzFyEI6ZTF1E8womFWg130_provenance
;
np:hasPublicationInfo
dgn-np:NP311593.RAFSbNjT4Bdih4nAUhIOyc263IIzFyEI6ZTF1E8womFWg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP311593.RAFSbNjT4Bdih4nAUhIOyc263IIzFyEI6ZTF1E8womFWg130_assertion
a
np:Assertion
.
dgn-np:NP311593.RAFSbNjT4Bdih4nAUhIOyc263IIzFyEI6ZTF1E8womFWg130_provenance
a
np:Provenance
.
dgn-np:NP311593.RAFSbNjT4Bdih4nAUhIOyc263IIzFyEI6ZTF1E8womFWg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP311593.RAFSbNjT4Bdih4nAUhIOyc263IIzFyEI6ZTF1E8womFWg130_assertion
{
miriam-gene:4709
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN9fd13ef7be9f831e7cd592b3146bcf44
sio:SIO_000628
miriam-gene:4709
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP311593.RAFSbNjT4Bdih4nAUhIOyc263IIzFyEI6ZTF1E8womFWg130_provenance
{
dgn-np:NP311593.RAFSbNjT4Bdih4nAUhIOyc263IIzFyEI6ZTF1E8womFWg130_assertion
dcterms:description
"[To examine the graded risks for coronary artery disease (CAD) associated with plasma homocyst(e)ine [H(e)] and to evaluate the extent to which this risk is mediated by altered vitamin status, we measured plasma concentrations of H(e), vitamins B6 and B12, and folate as well as other coronary risk factors in subjects with early familial CAD and in control subjects.]. 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:7670943
;
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:NP311593.RAFSbNjT4Bdih4nAUhIOyc263IIzFyEI6ZTF1E8womFWg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:58+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" .
}