@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP589290.RAjHYgHWbigqOmz1_CRUQnDoh264rmuNW4yDGTDQCPkxk
> .
@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:NP589290.RAjHYgHWbigqOmz1_CRUQnDoh264rmuNW4yDGTDQCPkxk130_head
{
this:
np:hasAssertion
dgn-np:NP589290.RAjHYgHWbigqOmz1_CRUQnDoh264rmuNW4yDGTDQCPkxk130_assertion
;
np:hasProvenance
dgn-np:NP589290.RAjHYgHWbigqOmz1_CRUQnDoh264rmuNW4yDGTDQCPkxk130_provenance
;
np:hasPublicationInfo
dgn-np:NP589290.RAjHYgHWbigqOmz1_CRUQnDoh264rmuNW4yDGTDQCPkxk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP589290.RAjHYgHWbigqOmz1_CRUQnDoh264rmuNW4yDGTDQCPkxk130_assertion
a
np:Assertion
.
dgn-np:NP589290.RAjHYgHWbigqOmz1_CRUQnDoh264rmuNW4yDGTDQCPkxk130_provenance
a
np:Provenance
.
dgn-np:NP589290.RAjHYgHWbigqOmz1_CRUQnDoh264rmuNW4yDGTDQCPkxk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP589290.RAjHYgHWbigqOmz1_CRUQnDoh264rmuNW4yDGTDQCPkxk130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0151744
a
ncit:C7057
.
dgn-gda:DGN49ec021ad5d02066813e996054450738
sio:SIO_000628
miriam-gene:4524
,
lld:C0151744
;
a
sio:SIO_001121
.
}
dgn-np:NP589290.RAjHYgHWbigqOmz1_CRUQnDoh264rmuNW4yDGTDQCPkxk130_provenance
{
dgn-np:NP589290.RAjHYgHWbigqOmz1_CRUQnDoh264rmuNW4yDGTDQCPkxk130_assertion
dcterms:description
"[Meta-analyses of ischaemic heart disease using (i) 75 studies in which the prevalence of a mutation (CT) in the MTHFR gene (which increases homocysteine) was determined in cases (22,068) and controls (23,618), and (ii) 14 randomised trials (39,597 participants) of homocysteine lowering and ischaemic heart disease events.]. 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:21311765
;
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:NP589290.RAjHYgHWbigqOmz1_CRUQnDoh264rmuNW4yDGTDQCPkxk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:54+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" .
}