@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP409069.RAIOlow3o_fn_nU3Cr2o840WhViaEEc0LsZWPRPoZaVRM
> .
@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:NP409069.RAIOlow3o_fn_nU3Cr2o840WhViaEEc0LsZWPRPoZaVRM130_head
{
this:
np:hasAssertion
dgn-np:NP409069.RAIOlow3o_fn_nU3Cr2o840WhViaEEc0LsZWPRPoZaVRM130_assertion
;
np:hasProvenance
dgn-np:NP409069.RAIOlow3o_fn_nU3Cr2o840WhViaEEc0LsZWPRPoZaVRM130_provenance
;
np:hasPublicationInfo
dgn-np:NP409069.RAIOlow3o_fn_nU3Cr2o840WhViaEEc0LsZWPRPoZaVRM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP409069.RAIOlow3o_fn_nU3Cr2o840WhViaEEc0LsZWPRPoZaVRM130_assertion
a
np:Assertion
.
dgn-np:NP409069.RAIOlow3o_fn_nU3Cr2o840WhViaEEc0LsZWPRPoZaVRM130_provenance
a
np:Provenance
.
dgn-np:NP409069.RAIOlow3o_fn_nU3Cr2o840WhViaEEc0LsZWPRPoZaVRM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP409069.RAIOlow3o_fn_nU3Cr2o840WhViaEEc0LsZWPRPoZaVRM130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0031106
a
ncit:C7057
.
dgn-gda:DGNe8cc67207e81123b867057acee9e41d7
sio:SIO_000628
miriam-gene:1029
,
lld:C0031106
;
a
sio:SIO_001121
.
}
dgn-np:NP409069.RAIOlow3o_fn_nU3Cr2o840WhViaEEc0LsZWPRPoZaVRM130_provenance
{
dgn-np:NP409069.RAIOlow3o_fn_nU3Cr2o840WhViaEEc0LsZWPRPoZaVRM130_assertion
dcterms:description
"[To identify and validate risk variants in different European populations, we first explored 150 kb of the genetic region of CDKN2BAS including the adjacent genes CDKN2A and CDKN2B, covering 51 tagging single nucleotide polymorphisms (tagSNPs) in AgP and chronic periodontitis (CP) in individuals of Dutch origin (n=313).]. 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:20978019
;
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:NP409069.RAIOlow3o_fn_nU3Cr2o840WhViaEEc0LsZWPRPoZaVRM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:03+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" .
}