@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP550682.RA35G64BcqsQto5ZbR_h-F-CJqhiwejGpsa3tGugO6UUE
> .
@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:NP550682.RA35G64BcqsQto5ZbR_h-F-CJqhiwejGpsa3tGugO6UUE130_head
{
this:
np:hasAssertion
dgn-np:NP550682.RA35G64BcqsQto5ZbR_h-F-CJqhiwejGpsa3tGugO6UUE130_assertion
;
np:hasProvenance
dgn-np:NP550682.RA35G64BcqsQto5ZbR_h-F-CJqhiwejGpsa3tGugO6UUE130_provenance
;
np:hasPublicationInfo
dgn-np:NP550682.RA35G64BcqsQto5ZbR_h-F-CJqhiwejGpsa3tGugO6UUE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP550682.RA35G64BcqsQto5ZbR_h-F-CJqhiwejGpsa3tGugO6UUE130_assertion
a
np:Assertion
.
dgn-np:NP550682.RA35G64BcqsQto5ZbR_h-F-CJqhiwejGpsa3tGugO6UUE130_provenance
a
np:Provenance
.
dgn-np:NP550682.RA35G64BcqsQto5ZbR_h-F-CJqhiwejGpsa3tGugO6UUE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP550682.RA35G64BcqsQto5ZbR_h-F-CJqhiwejGpsa3tGugO6UUE130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0040136
a
ncit:C7057
.
dgn-gda:DGN08fc3b32589d43f0bab9d3051dfa3a4c
sio:SIO_000628
miriam-gene:5728
,
lld:C0040136
;
a
sio:SIO_001121
.
}
dgn-np:NP550682.RA35G64BcqsQto5ZbR_h-F-CJqhiwejGpsa3tGugO6UUE130_provenance
{
dgn-np:NP550682.RA35G64BcqsQto5ZbR_h-F-CJqhiwejGpsa3tGugO6UUE130_assertion
dcterms:description
"[Somatic PTEN deletions and mutations were observed in sporadic breast, brain, prostate and kidney cancer cell lines and in several primary tumours such as endometrial carcinomas, malignant melanoma and thyroid tumours.]. 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:9467011
;
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:NP550682.RA35G64BcqsQto5ZbR_h-F-CJqhiwejGpsa3tGugO6UUE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:32+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" .
}