@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP469993.RAkDbJgbFv_I7Xv3L2kWXcvUOAyOuF7duhJcrpemA6emU
> .
@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:NP469993.RAkDbJgbFv_I7Xv3L2kWXcvUOAyOuF7duhJcrpemA6emU130_head
{
this:
np:hasAssertion
dgn-np:NP469993.RAkDbJgbFv_I7Xv3L2kWXcvUOAyOuF7duhJcrpemA6emU130_assertion
;
np:hasProvenance
dgn-np:NP469993.RAkDbJgbFv_I7Xv3L2kWXcvUOAyOuF7duhJcrpemA6emU130_provenance
;
np:hasPublicationInfo
dgn-np:NP469993.RAkDbJgbFv_I7Xv3L2kWXcvUOAyOuF7duhJcrpemA6emU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP469993.RAkDbJgbFv_I7Xv3L2kWXcvUOAyOuF7duhJcrpemA6emU130_assertion
a
np:Assertion
.
dgn-np:NP469993.RAkDbJgbFv_I7Xv3L2kWXcvUOAyOuF7duhJcrpemA6emU130_provenance
a
np:Provenance
.
dgn-np:NP469993.RAkDbJgbFv_I7Xv3L2kWXcvUOAyOuF7duhJcrpemA6emU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP469993.RAkDbJgbFv_I7Xv3L2kWXcvUOAyOuF7duhJcrpemA6emU130_assertion
{
miriam-gene:1030
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN28e048fa8a0ef6dc2536e9eaac325bb7
sio:SIO_000628
miriam-gene:1030
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP469993.RAkDbJgbFv_I7Xv3L2kWXcvUOAyOuF7duhJcrpemA6emU130_provenance
{
dgn-np:NP469993.RAkDbJgbFv_I7Xv3L2kWXcvUOAyOuF7duhJcrpemA6emU130_assertion
dcterms:description
"[The results of this study indicate that the 9p21 variation has an impact on CDKN2A and CDKN2B expression in VSMCs and influences VMSC proliferation, which likely represents an important mechanism for the association between this genetic locus and susceptibility to CAD.]. 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:22706276
;
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:NP469993.RAkDbJgbFv_I7Xv3L2kWXcvUOAyOuF7duhJcrpemA6emU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:42+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" .
}