@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP907820.RAkeQzdGJEIWPZTjBBaB8V8L5Z0d348tR_l3OD5ethLyc
> .
@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:NP907820.RAkeQzdGJEIWPZTjBBaB8V8L5Z0d348tR_l3OD5ethLyc130_head
{
this:
np:hasAssertion
dgn-np:NP907820.RAkeQzdGJEIWPZTjBBaB8V8L5Z0d348tR_l3OD5ethLyc130_assertion
;
np:hasProvenance
dgn-np:NP907820.RAkeQzdGJEIWPZTjBBaB8V8L5Z0d348tR_l3OD5ethLyc130_provenance
;
np:hasPublicationInfo
dgn-np:NP907820.RAkeQzdGJEIWPZTjBBaB8V8L5Z0d348tR_l3OD5ethLyc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP907820.RAkeQzdGJEIWPZTjBBaB8V8L5Z0d348tR_l3OD5ethLyc130_assertion
a
np:Assertion
.
dgn-np:NP907820.RAkeQzdGJEIWPZTjBBaB8V8L5Z0d348tR_l3OD5ethLyc130_provenance
a
np:Provenance
.
dgn-np:NP907820.RAkeQzdGJEIWPZTjBBaB8V8L5Z0d348tR_l3OD5ethLyc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP907820.RAkeQzdGJEIWPZTjBBaB8V8L5Z0d348tR_l3OD5ethLyc130_assertion
{
miriam-gene:5520
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNe4f98ad3d71b8bf966a2492ca29d343c
sio:SIO_000628
miriam-gene:5520
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP907820.RAkeQzdGJEIWPZTjBBaB8V8L5Z0d348tR_l3OD5ethLyc130_provenance
{
dgn-np:NP907820.RAkeQzdGJEIWPZTjBBaB8V8L5Z0d348tR_l3OD5ethLyc130_assertion
dcterms:description
"[The effects of haplotypes for 2 PP2A regulatory subunit genes, PP2 regulatory subunit B alpha isoform (PPP2R2A) and PP2A regulatory subunit B' epsilon isoform (PPP2R5E) on breast cancer risk were nominally significant but did not remain significant after the analysis was adjusted for multiple comparisons.]. 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:19890961
;
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:NP907820.RAkeQzdGJEIWPZTjBBaB8V8L5Z0d348tR_l3OD5ethLyc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:17+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" .
}