@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP801594.RAFu4AXul0OGlm2ZDFC1w_eOid2IyL2lpzTh1pQSBAMgM
> .
@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:NP801594.RAFu4AXul0OGlm2ZDFC1w_eOid2IyL2lpzTh1pQSBAMgM130_head
{
this:
np:hasAssertion
dgn-np:NP801594.RAFu4AXul0OGlm2ZDFC1w_eOid2IyL2lpzTh1pQSBAMgM130_assertion
;
np:hasProvenance
dgn-np:NP801594.RAFu4AXul0OGlm2ZDFC1w_eOid2IyL2lpzTh1pQSBAMgM130_provenance
;
np:hasPublicationInfo
dgn-np:NP801594.RAFu4AXul0OGlm2ZDFC1w_eOid2IyL2lpzTh1pQSBAMgM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP801594.RAFu4AXul0OGlm2ZDFC1w_eOid2IyL2lpzTh1pQSBAMgM130_assertion
a
np:Assertion
.
dgn-np:NP801594.RAFu4AXul0OGlm2ZDFC1w_eOid2IyL2lpzTh1pQSBAMgM130_provenance
a
np:Provenance
.
dgn-np:NP801594.RAFu4AXul0OGlm2ZDFC1w_eOid2IyL2lpzTh1pQSBAMgM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP801594.RAFu4AXul0OGlm2ZDFC1w_eOid2IyL2lpzTh1pQSBAMgM130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN019d1e5e33bc3b8261d4b5bb1dd095c7
sio:SIO_000628
miriam-gene:5728
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP801594.RAFu4AXul0OGlm2ZDFC1w_eOid2IyL2lpzTh1pQSBAMgM130_provenance
{
dgn-np:NP801594.RAFu4AXul0OGlm2ZDFC1w_eOid2IyL2lpzTh1pQSBAMgM130_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_literature
;
sio:SIO_000772
miriam-pubmed:12085208
;
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:NP801594.RAFu4AXul0OGlm2ZDFC1w_eOid2IyL2lpzTh1pQSBAMgM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:12+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" .
}