@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP606499.RAk3z_d2vSKSK9a5NSAjqAgoTLv_zyIhAjFrQvJOtV4Is
> .
@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:NP606499.RAk3z_d2vSKSK9a5NSAjqAgoTLv_zyIhAjFrQvJOtV4Is130_head
{
this:
np:hasAssertion
dgn-np:NP606499.RAk3z_d2vSKSK9a5NSAjqAgoTLv_zyIhAjFrQvJOtV4Is130_assertion
;
np:hasProvenance
dgn-np:NP606499.RAk3z_d2vSKSK9a5NSAjqAgoTLv_zyIhAjFrQvJOtV4Is130_provenance
;
np:hasPublicationInfo
dgn-np:NP606499.RAk3z_d2vSKSK9a5NSAjqAgoTLv_zyIhAjFrQvJOtV4Is130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP606499.RAk3z_d2vSKSK9a5NSAjqAgoTLv_zyIhAjFrQvJOtV4Is130_assertion
a
np:Assertion
.
dgn-np:NP606499.RAk3z_d2vSKSK9a5NSAjqAgoTLv_zyIhAjFrQvJOtV4Is130_provenance
a
np:Provenance
.
dgn-np:NP606499.RAk3z_d2vSKSK9a5NSAjqAgoTLv_zyIhAjFrQvJOtV4Is130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP606499.RAk3z_d2vSKSK9a5NSAjqAgoTLv_zyIhAjFrQvJOtV4Is130_assertion
{
miriam-gene:100048912
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN0939ebd0e0c2490f128bdf25992ef237
sio:SIO_000628
miriam-gene:100048912
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP606499.RAk3z_d2vSKSK9a5NSAjqAgoTLv_zyIhAjFrQvJOtV4Is130_provenance
{
dgn-np:NP606499.RAk3z_d2vSKSK9a5NSAjqAgoTLv_zyIhAjFrQvJOtV4Is130_assertion
dcterms:description
"[We have investigated the functional significance of conserved sequences within the 9p21.3 risk locus for coronary artery disease (CAD) and determined the relationship of 9p21.3 to expression of ANRIL and to whole genome gene expression.]. 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:19592466
;
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:NP606499.RAk3z_d2vSKSK9a5NSAjqAgoTLv_zyIhAjFrQvJOtV4Is130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:04+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" .
}