@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP570515.RAb9_a0cl2hG4DbNXGl56geBEoXE1yNDUUpr2fhgMYYQw
> .
@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:NP570515.RAb9_a0cl2hG4DbNXGl56geBEoXE1yNDUUpr2fhgMYYQw130_head
{
this:
np:hasAssertion
dgn-np:NP570515.RAb9_a0cl2hG4DbNXGl56geBEoXE1yNDUUpr2fhgMYYQw130_assertion
;
np:hasProvenance
dgn-np:NP570515.RAb9_a0cl2hG4DbNXGl56geBEoXE1yNDUUpr2fhgMYYQw130_provenance
;
np:hasPublicationInfo
dgn-np:NP570515.RAb9_a0cl2hG4DbNXGl56geBEoXE1yNDUUpr2fhgMYYQw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP570515.RAb9_a0cl2hG4DbNXGl56geBEoXE1yNDUUpr2fhgMYYQw130_assertion
a
np:Assertion
.
dgn-np:NP570515.RAb9_a0cl2hG4DbNXGl56geBEoXE1yNDUUpr2fhgMYYQw130_provenance
a
np:Provenance
.
dgn-np:NP570515.RAb9_a0cl2hG4DbNXGl56geBEoXE1yNDUUpr2fhgMYYQw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP570515.RAb9_a0cl2hG4DbNXGl56geBEoXE1yNDUUpr2fhgMYYQw130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGNedf696f4343fc6689447191e592192bb
sio:SIO_000628
miriam-gene:5728
,
lld:C0026764
;
a
sio:SIO_001121
.
}
dgn-np:NP570515.RAb9_a0cl2hG4DbNXGl56geBEoXE1yNDUUpr2fhgMYYQw130_provenance
{
dgn-np:NP570515.RAb9_a0cl2hG4DbNXGl56geBEoXE1yNDUUpr2fhgMYYQw130_assertion
dcterms:description
"[Our results indicate that alterations of PTEN are uncommon in MM patients, and PTEN deletions tend to occur in advanced disease suggesting that they are secondary, rather than primary, events in the pathogenesis of MM.]. 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:16112193
;
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:NP570515.RAb9_a0cl2hG4DbNXGl56geBEoXE1yNDUUpr2fhgMYYQw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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" .
}