@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP423883.RARLhw_vt8PKhPFAoqYsX9rp9yoaDUY7heT7ZBPcb4q3M
> .
@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:NP423883.RARLhw_vt8PKhPFAoqYsX9rp9yoaDUY7heT7ZBPcb4q3M130_head
{
this:
np:hasAssertion
dgn-np:NP423883.RARLhw_vt8PKhPFAoqYsX9rp9yoaDUY7heT7ZBPcb4q3M130_assertion
;
np:hasProvenance
dgn-np:NP423883.RARLhw_vt8PKhPFAoqYsX9rp9yoaDUY7heT7ZBPcb4q3M130_provenance
;
np:hasPublicationInfo
dgn-np:NP423883.RARLhw_vt8PKhPFAoqYsX9rp9yoaDUY7heT7ZBPcb4q3M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP423883.RARLhw_vt8PKhPFAoqYsX9rp9yoaDUY7heT7ZBPcb4q3M130_assertion
a
np:Assertion
.
dgn-np:NP423883.RARLhw_vt8PKhPFAoqYsX9rp9yoaDUY7heT7ZBPcb4q3M130_provenance
a
np:Provenance
.
dgn-np:NP423883.RARLhw_vt8PKhPFAoqYsX9rp9yoaDUY7heT7ZBPcb4q3M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP423883.RARLhw_vt8PKhPFAoqYsX9rp9yoaDUY7heT7ZBPcb4q3M130_assertion
{
miriam-gene:5524
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGNae57451b0ac38d398a2a681c6ba3c0e3
sio:SIO_000628
miriam-gene:5524
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP423883.RARLhw_vt8PKhPFAoqYsX9rp9yoaDUY7heT7ZBPcb4q3M130_provenance
{
dgn-np:NP423883.RARLhw_vt8PKhPFAoqYsX9rp9yoaDUY7heT7ZBPcb4q3M130_assertion
dcterms:description
"[Although the frequency of alterations is low, the inclusion of both isoforms of subunit A in the genes mutated in human cancer and the addition of breast cancer to the list of neoplasms in which PPP2R1B is altered, strengthen the potential role of PP2A in human tumorogenesis.]. 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:10713707
;
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:NP423883.RARLhw_vt8PKhPFAoqYsX9rp9yoaDUY7heT7ZBPcb4q3M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:11+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" .
}