@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP232549.RAod-2mrMWj0lGWoz2Sw45Ng-nJpqZSSFLEJcjJN-yfPg
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP232549.RAod-2mrMWj0lGWoz2Sw45Ng-nJpqZSSFLEJcjJN-yfPg130_assertion
;
np:hasProvenance
dgn-np:NP232549.RAod-2mrMWj0lGWoz2Sw45Ng-nJpqZSSFLEJcjJN-yfPg130_provenance
;
np:hasPublicationInfo
dgn-np:NP232549.RAod-2mrMWj0lGWoz2Sw45Ng-nJpqZSSFLEJcjJN-yfPg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP232549.RAod-2mrMWj0lGWoz2Sw45Ng-nJpqZSSFLEJcjJN-yfPg130_assertion
a
np:Assertion
.
dgn-np:NP232549.RAod-2mrMWj0lGWoz2Sw45Ng-nJpqZSSFLEJcjJN-yfPg130_provenance
a
np:Provenance
.
dgn-np:NP232549.RAod-2mrMWj0lGWoz2Sw45Ng-nJpqZSSFLEJcjJN-yfPg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP232549.RAod-2mrMWj0lGWoz2Sw45Ng-nJpqZSSFLEJcjJN-yfPg130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0334108
a
ncit:C7057
.
dgn-gda:DGNa5fed98d74b92f68e449b251d675957b
sio:SIO_000628
miriam-gene:324
,
lld:C0334108
;
a
sio:SIO_001121
.
}
dgn-np:NP232549.RAod-2mrMWj0lGWoz2Sw45Ng-nJpqZSSFLEJcjJN-yfPg130_provenance
{
dgn-np:NP232549.RAod-2mrMWj0lGWoz2Sw45Ng-nJpqZSSFLEJcjJN-yfPg130_assertion
dcterms:description
"[The findings demonstrate the value of the PTT in identifying mosaic mutations in apparently APC mutation negative FAP patients with de novo classical polyposis and the need to keep the PTT within the diagnostic repertoire for APC mutation analysis.]. 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:21653199
;
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 .
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dgn-np:NP232549.RAod-2mrMWj0lGWoz2Sw45Ng-nJpqZSSFLEJcjJN-yfPg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:10+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" .
}