@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP27571.RAz23pjy4RD7JoMMEiWt0jG1k2VBarKTGCuDBzw2CVt8k
> .
@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:NP27571.RAz23pjy4RD7JoMMEiWt0jG1k2VBarKTGCuDBzw2CVt8k130_head
{
this:
np:hasAssertion
dgn-np:NP27571.RAz23pjy4RD7JoMMEiWt0jG1k2VBarKTGCuDBzw2CVt8k130_assertion
;
np:hasProvenance
dgn-np:NP27571.RAz23pjy4RD7JoMMEiWt0jG1k2VBarKTGCuDBzw2CVt8k130_provenance
;
np:hasPublicationInfo
dgn-np:NP27571.RAz23pjy4RD7JoMMEiWt0jG1k2VBarKTGCuDBzw2CVt8k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP27571.RAz23pjy4RD7JoMMEiWt0jG1k2VBarKTGCuDBzw2CVt8k130_assertion
a
np:Assertion
.
dgn-np:NP27571.RAz23pjy4RD7JoMMEiWt0jG1k2VBarKTGCuDBzw2CVt8k130_provenance
a
np:Provenance
.
dgn-np:NP27571.RAz23pjy4RD7JoMMEiWt0jG1k2VBarKTGCuDBzw2CVt8k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP27571.RAz23pjy4RD7JoMMEiWt0jG1k2VBarKTGCuDBzw2CVt8k130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0025286
a
ncit:C7057
.
dgn-gda:DGN2304191cd963e254b436cee1e4d1ce5d
sio:SIO_000628
miriam-gene:5728
,
lld:C0025286
;
a
sio:SIO_001121
.
}
dgn-np:NP27571.RAz23pjy4RD7JoMMEiWt0jG1k2VBarKTGCuDBzw2CVt8k130_provenance
{
dgn-np:NP27571.RAz23pjy4RD7JoMMEiWt0jG1k2VBarKTGCuDBzw2CVt8k130_assertion
dcterms: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:NP27571.RAz23pjy4RD7JoMMEiWt0jG1k2VBarKTGCuDBzw2CVt8k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:11+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" .
}