@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_head
{
this:
np:hasAssertion
dgn-np:NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_assertion
;
np:hasProvenance
dgn-np:NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_provenance
;
np:hasPublicationInfo
dgn-np:NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_assertion
a
np:Assertion
.
dgn-np:NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_provenance
a
np:Provenance
.
dgn-np:NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0549473
a
ncit:C7057
.
dgn-gda:DGN88db4e0ee0e7948847ecaf5701cc2df9
sio:SIO_000628
miriam-gene:7248
,
lld:C0549473
;
a
sio:SIO_001121
.
}
dgn-np:NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_provenance
{
dgn-np:NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_assertion
dcterms:description
"[PTEN hamartoma tumour syndrome (PHTS) encompasses several clinical syndromes with germline mutations in the PTEN tumour suppressor gene, including Cowden syndrome which is characterised by an increased risk of breast and thyroid cancers.]. 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:23335809
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP759534.RAd3_L7LK9yRhsip9zmF6Nbc_l9OhyADm4fOjlW4V5ia0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:18+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}