@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw
> .
@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 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:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_head
{
this:
np:hasAssertion
dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_assertion
;
np:hasProvenance
dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_provenance
;
np:hasPublicationInfo
dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_assertion
a
np:Assertion
.
dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_provenance
a
np:Provenance
.
dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGN6465dcc27c1771efca22b428aa75c1ba
sio:SIO_000628
miriam-gene:5728
,
lld:C0017638
;
a
sio:SIO_001121
.
}
dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_provenance
{
dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_assertion
dct:description
"[The reported patient, in addition to glioma, had suffered from benign meningioma in the past but did not show any clinical signs of Cowden disease or other hereditary diseases typically associated with PTEN germline mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:12085208
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:11+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}