@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP206538.RA9gq7zPbSxpWFOydya5WRgVG5VEH2JSRcjEzotI8awLc
> .
@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:NP206538.RA9gq7zPbSxpWFOydya5WRgVG5VEH2JSRcjEzotI8awLc130_head
{
this:
np:hasAssertion
dgn-np:NP206538.RA9gq7zPbSxpWFOydya5WRgVG5VEH2JSRcjEzotI8awLc130_assertion
;
np:hasProvenance
dgn-np:NP206538.RA9gq7zPbSxpWFOydya5WRgVG5VEH2JSRcjEzotI8awLc130_provenance
;
np:hasPublicationInfo
dgn-np:NP206538.RA9gq7zPbSxpWFOydya5WRgVG5VEH2JSRcjEzotI8awLc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP206538.RA9gq7zPbSxpWFOydya5WRgVG5VEH2JSRcjEzotI8awLc130_assertion
a
np:Assertion
.
dgn-np:NP206538.RA9gq7zPbSxpWFOydya5WRgVG5VEH2JSRcjEzotI8awLc130_provenance
a
np:Provenance
.
dgn-np:NP206538.RA9gq7zPbSxpWFOydya5WRgVG5VEH2JSRcjEzotI8awLc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP206538.RA9gq7zPbSxpWFOydya5WRgVG5VEH2JSRcjEzotI8awLc130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0018553
a
ncit:C7057
.
dgn-gda:DGNf4de27d7384acd0181abed35ecd51014
sio:SIO_000628
miriam-gene:5728
,
lld:C0018553
;
a
sio:SIO_001121
.
}
dgn-np:NP206538.RA9gq7zPbSxpWFOydya5WRgVG5VEH2JSRcjEzotI8awLc130_provenance
{
dgn-np:NP206538.RA9gq7zPbSxpWFOydya5WRgVG5VEH2JSRcjEzotI8awLc130_assertion
dcterms:description
"[This observation suggests that Cowden disease patients are not only at risk for additional tumorigenic mutations due to complete loss of PTEN function, but may also experience accelerated growth of incipient tumours due to enhanced angiogenesis.]. 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:17371230
;
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:NP206538.RA9gq7zPbSxpWFOydya5WRgVG5VEH2JSRcjEzotI8awLc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:54+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" .
}