@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc
> .
@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:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_head
{
this:
np:hasAssertion
dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_assertion
;
np:hasProvenance
dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_provenance
;
np:hasPublicationInfo
dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_assertion
a
np:Assertion
.
dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_provenance
a
np:Provenance
.
dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0018552
a
ncit:C7057
.
dgn-gda:DGN0d2c5eddde09b0d9bd612f4045f0ab89
sio:SIO_000628
miriam-gene:5728
,
lld:C0018552
;
a
sio:SIO_001121
.
}
dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_provenance
{
dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_assertion
dcterms:description
"[Taken together, our findings indicate that benign hamartomas in CD may develop without loss of the second (wild-type) PTEN allele, whereas the pathogenesis of malignant tumours, such as breast carcinomas, appears to require the complete inactivation of Pten as well as further alterations such as the loss of p53-dependent growth control.]. 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:12786840
;
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:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}