@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP761923.RAkp0SHOntJ-Hc6hGSCsm2-n8Nc8gWODdECeecsTtjigI
> .
@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:NP761923.RAkp0SHOntJ-Hc6hGSCsm2-n8Nc8gWODdECeecsTtjigI130_head
{
this:
np:hasAssertion
dgn-np:NP761923.RAkp0SHOntJ-Hc6hGSCsm2-n8Nc8gWODdECeecsTtjigI130_assertion
;
np:hasProvenance
dgn-np:NP761923.RAkp0SHOntJ-Hc6hGSCsm2-n8Nc8gWODdECeecsTtjigI130_provenance
;
np:hasPublicationInfo
dgn-np:NP761923.RAkp0SHOntJ-Hc6hGSCsm2-n8Nc8gWODdECeecsTtjigI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP761923.RAkp0SHOntJ-Hc6hGSCsm2-n8Nc8gWODdECeecsTtjigI130_assertion
a
np:Assertion
.
dgn-np:NP761923.RAkp0SHOntJ-Hc6hGSCsm2-n8Nc8gWODdECeecsTtjigI130_provenance
a
np:Provenance
.
dgn-np:NP761923.RAkp0SHOntJ-Hc6hGSCsm2-n8Nc8gWODdECeecsTtjigI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP761923.RAkp0SHOntJ-Hc6hGSCsm2-n8Nc8gWODdECeecsTtjigI130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C1333600
a
ncit:C7057
.
dgn-gda:DGN18b13639528555d645578e9225328fb1
sio:SIO_000628
miriam-gene:5728
,
lld:C1333600
;
a
sio:SIO_001121
.
}
dgn-np:NP761923.RAkp0SHOntJ-Hc6hGSCsm2-n8Nc8gWODdECeecsTtjigI130_provenance
{
dgn-np:NP761923.RAkp0SHOntJ-Hc6hGSCsm2-n8Nc8gWODdECeecsTtjigI130_assertion
dcterms:description
"[PTEN activity is lost by mutations, deletions or promoter methylation at high frequency in many primary and metastatic human cancers, and some germline mutations of PTEN are found in several familial cancer predisposition syndromes.]. 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:20214616
;
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:NP761923.RAkp0SHOntJ-Hc6hGSCsm2-n8Nc8gWODdECeecsTtjigI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:41+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" .
}