@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP921789.RA9FZycOrk18gn3D2Y3dl8DO6rmo0otp9JbhzBuaX3BL8
> .
@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:NP921789.RA9FZycOrk18gn3D2Y3dl8DO6rmo0otp9JbhzBuaX3BL8130_head
{
this:
np:hasAssertion
dgn-np:NP921789.RA9FZycOrk18gn3D2Y3dl8DO6rmo0otp9JbhzBuaX3BL8130_assertion
;
np:hasProvenance
dgn-np:NP921789.RA9FZycOrk18gn3D2Y3dl8DO6rmo0otp9JbhzBuaX3BL8130_provenance
;
np:hasPublicationInfo
dgn-np:NP921789.RA9FZycOrk18gn3D2Y3dl8DO6rmo0otp9JbhzBuaX3BL8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP921789.RA9FZycOrk18gn3D2Y3dl8DO6rmo0otp9JbhzBuaX3BL8130_assertion
a
np:Assertion
.
dgn-np:NP921789.RA9FZycOrk18gn3D2Y3dl8DO6rmo0otp9JbhzBuaX3BL8130_provenance
a
np:Provenance
.
dgn-np:NP921789.RA9FZycOrk18gn3D2Y3dl8DO6rmo0otp9JbhzBuaX3BL8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP921789.RA9FZycOrk18gn3D2Y3dl8DO6rmo0otp9JbhzBuaX3BL8130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0347266
a
ncit:C7057
.
dgn-gda:DGNb29b9645cf11def327d610b2a1067333
sio:SIO_000628
miriam-gene:324
,
lld:C0347266
;
a
sio:SIO_001121
.
}
dgn-np:NP921789.RA9FZycOrk18gn3D2Y3dl8DO6rmo0otp9JbhzBuaX3BL8130_provenance
{
dgn-np:NP921789.RA9FZycOrk18gn3D2Y3dl8DO6rmo0otp9JbhzBuaX3BL8130_assertion
dcterms:description
"[Germline mutations in the APC gene are responsible for familial adenomatous polyposis (FAP), a dominantly inherited syndrome characterized by the development of hundreds to thousands of polyps in the colon and in the rectum of affected individuals and by variable extracolonic manifestations (gastric and duodenal polyps, osteomas, retinal lesions, and desmoid tumors).]. 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:10094547
;
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:NP921789.RA9FZycOrk18gn3D2Y3dl8DO6rmo0otp9JbhzBuaX3BL8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:25+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" .
}