@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP744183.RAPuNO8OHiBe5CCHhMRUjKEm6iH29wDOgAWOgJwYneuSE
> .
@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:NP744183.RAPuNO8OHiBe5CCHhMRUjKEm6iH29wDOgAWOgJwYneuSE130_head
{
this:
np:hasAssertion
dgn-np:NP744183.RAPuNO8OHiBe5CCHhMRUjKEm6iH29wDOgAWOgJwYneuSE130_assertion
;
np:hasProvenance
dgn-np:NP744183.RAPuNO8OHiBe5CCHhMRUjKEm6iH29wDOgAWOgJwYneuSE130_provenance
;
np:hasPublicationInfo
dgn-np:NP744183.RAPuNO8OHiBe5CCHhMRUjKEm6iH29wDOgAWOgJwYneuSE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP744183.RAPuNO8OHiBe5CCHhMRUjKEm6iH29wDOgAWOgJwYneuSE130_assertion
a
np:Assertion
.
dgn-np:NP744183.RAPuNO8OHiBe5CCHhMRUjKEm6iH29wDOgAWOgJwYneuSE130_provenance
a
np:Provenance
.
dgn-np:NP744183.RAPuNO8OHiBe5CCHhMRUjKEm6iH29wDOgAWOgJwYneuSE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP744183.RAPuNO8OHiBe5CCHhMRUjKEm6iH29wDOgAWOgJwYneuSE130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0007112
a
ncit:C7057
.
dgn-gda:DGN19c1f5c4c9af1414f8b7b324077a86b5
sio:SIO_000628
miriam-gene:5728
,
lld:C0007112
;
a
sio:SIO_001121
.
}
dgn-np:NP744183.RAPuNO8OHiBe5CCHhMRUjKEm6iH29wDOgAWOgJwYneuSE130_provenance
{
dgn-np:NP744183.RAPuNO8OHiBe5CCHhMRUjKEm6iH29wDOgAWOgJwYneuSE130_assertion
dcterms:description
"[Functional loss of the tumour suppressor phosphatase and tensin homologue deleted on chromosome ten (PTEN) and subsequent activation of the AKT pathway, have been prominently implicated in the progression of CaP to androgen-independence.]. 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:11901476
;
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:NP744183.RAPuNO8OHiBe5CCHhMRUjKEm6iH29wDOgAWOgJwYneuSE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:31+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" .
}