@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP362447.RAYxQpxB4QLB64flfdqmNtYUgwRCo55ptgqNkOmum_Yrw
> .
@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:NP362447.RAYxQpxB4QLB64flfdqmNtYUgwRCo55ptgqNkOmum_Yrw130_head
{
this:
np:hasAssertion
dgn-np:NP362447.RAYxQpxB4QLB64flfdqmNtYUgwRCo55ptgqNkOmum_Yrw130_assertion
;
np:hasProvenance
dgn-np:NP362447.RAYxQpxB4QLB64flfdqmNtYUgwRCo55ptgqNkOmum_Yrw130_provenance
;
np:hasPublicationInfo
dgn-np:NP362447.RAYxQpxB4QLB64flfdqmNtYUgwRCo55ptgqNkOmum_Yrw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP362447.RAYxQpxB4QLB64flfdqmNtYUgwRCo55ptgqNkOmum_Yrw130_assertion
a
np:Assertion
.
dgn-np:NP362447.RAYxQpxB4QLB64flfdqmNtYUgwRCo55ptgqNkOmum_Yrw130_provenance
a
np:Provenance
.
dgn-np:NP362447.RAYxQpxB4QLB64flfdqmNtYUgwRCo55ptgqNkOmum_Yrw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP362447.RAYxQpxB4QLB64flfdqmNtYUgwRCo55ptgqNkOmum_Yrw130_assertion
{
miriam-gene:79001
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNc435247806026270fc958725fd0a1feb
sio:SIO_000628
miriam-gene:79001
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP362447.RAYxQpxB4QLB64flfdqmNtYUgwRCo55ptgqNkOmum_Yrw130_provenance
{
dgn-np:NP362447.RAYxQpxB4QLB64flfdqmNtYUgwRCo55ptgqNkOmum_Yrw130_assertion
dcterms:description
"[It was the objective of this study to analyse the VKORC1 genotype frequency in patients with CHD and controls from Northern Germany and to investigate the association of VKORC1 and CHD risk in patients with an European background.]. 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:17549303
;
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:NP362447.RAYxQpxB4QLB64flfdqmNtYUgwRCo55ptgqNkOmum_Yrw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:32+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" .
}