@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP686374.RA48mTR28m_Zg78t2_HxN0KITFRQWHM06UUGTrQfZVGAo
> .
@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:NP686374.RA48mTR28m_Zg78t2_HxN0KITFRQWHM06UUGTrQfZVGAo130_head
{
this:
np:hasAssertion
dgn-np:NP686374.RA48mTR28m_Zg78t2_HxN0KITFRQWHM06UUGTrQfZVGAo130_assertion
;
np:hasProvenance
dgn-np:NP686374.RA48mTR28m_Zg78t2_HxN0KITFRQWHM06UUGTrQfZVGAo130_provenance
;
np:hasPublicationInfo
dgn-np:NP686374.RA48mTR28m_Zg78t2_HxN0KITFRQWHM06UUGTrQfZVGAo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP686374.RA48mTR28m_Zg78t2_HxN0KITFRQWHM06UUGTrQfZVGAo130_assertion
a
np:Assertion
.
dgn-np:NP686374.RA48mTR28m_Zg78t2_HxN0KITFRQWHM06UUGTrQfZVGAo130_provenance
a
np:Provenance
.
dgn-np:NP686374.RA48mTR28m_Zg78t2_HxN0KITFRQWHM06UUGTrQfZVGAo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP686374.RA48mTR28m_Zg78t2_HxN0KITFRQWHM06UUGTrQfZVGAo130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C1832526
a
ncit:C7057
.
dgn-gda:DGN20801c6ff700604c0ee3a24d2af472f6
sio:SIO_000628
miriam-gene:5728
,
lld:C1832526
;
a
sio:SIO_001121
.
}
dgn-np:NP686374.RA48mTR28m_Zg78t2_HxN0KITFRQWHM06UUGTrQfZVGAo130_provenance
{
dgn-np:NP686374.RA48mTR28m_Zg78t2_HxN0KITFRQWHM06UUGTrQfZVGAo130_assertion
dcterms:description
"[This study therefore evaluated whether inactivation of PTEN may be involved in the tumourigenesis of PCC in man and whether PTEN abnormalities may help to define the malignant potential of these 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:16538614
;
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:NP686374.RA48mTR28m_Zg78t2_HxN0KITFRQWHM06UUGTrQfZVGAo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:57+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" .
}