@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP420649.RA-NDdLVfdi3q30f8PFHeZxC2x4xCxtkQPwkE-n2mVtzc
> .
@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:NP420649.RA-NDdLVfdi3q30f8PFHeZxC2x4xCxtkQPwkE-n2mVtzc130_head
{
this:
np:hasAssertion
dgn-np:NP420649.RA-NDdLVfdi3q30f8PFHeZxC2x4xCxtkQPwkE-n2mVtzc130_assertion
;
np:hasProvenance
dgn-np:NP420649.RA-NDdLVfdi3q30f8PFHeZxC2x4xCxtkQPwkE-n2mVtzc130_provenance
;
np:hasPublicationInfo
dgn-np:NP420649.RA-NDdLVfdi3q30f8PFHeZxC2x4xCxtkQPwkE-n2mVtzc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP420649.RA-NDdLVfdi3q30f8PFHeZxC2x4xCxtkQPwkE-n2mVtzc130_assertion
a
np:Assertion
.
dgn-np:NP420649.RA-NDdLVfdi3q30f8PFHeZxC2x4xCxtkQPwkE-n2mVtzc130_provenance
a
np:Provenance
.
dgn-np:NP420649.RA-NDdLVfdi3q30f8PFHeZxC2x4xCxtkQPwkE-n2mVtzc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP420649.RA-NDdLVfdi3q30f8PFHeZxC2x4xCxtkQPwkE-n2mVtzc130_assertion
{
miriam-gene:4830
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN598aa37d5aab47de3e80a9d7ac1132bb
sio:SIO_000628
miriam-gene:4830
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP420649.RA-NDdLVfdi3q30f8PFHeZxC2x4xCxtkQPwkE-n2mVtzc130_provenance
{
dgn-np:NP420649.RA-NDdLVfdi3q30f8PFHeZxC2x4xCxtkQPwkE-n2mVtzc130_assertion
dcterms:description
"[Using data from the Wellcome Trust Case Control Consortium, 1991 individuals with coronary artery disease (CAD) and 1500 controls from the UK Blood Services (NBS) were genotyped on the Affymetrix 500K array.]. 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:20676071
;
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:NP420649.RA-NDdLVfdi3q30f8PFHeZxC2x4xCxtkQPwkE-n2mVtzc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:09+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" .
}