@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP173581.RAuD7XI-vo32in1yyP8m9tFs9LGRmeG5Z7gYMinMy7VUI
> .
@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:NP173581.RAuD7XI-vo32in1yyP8m9tFs9LGRmeG5Z7gYMinMy7VUI130_head
{
this:
np:hasAssertion
dgn-np:NP173581.RAuD7XI-vo32in1yyP8m9tFs9LGRmeG5Z7gYMinMy7VUI130_assertion
;
np:hasProvenance
dgn-np:NP173581.RAuD7XI-vo32in1yyP8m9tFs9LGRmeG5Z7gYMinMy7VUI130_provenance
;
np:hasPublicationInfo
dgn-np:NP173581.RAuD7XI-vo32in1yyP8m9tFs9LGRmeG5Z7gYMinMy7VUI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP173581.RAuD7XI-vo32in1yyP8m9tFs9LGRmeG5Z7gYMinMy7VUI130_assertion
a
np:Assertion
.
dgn-np:NP173581.RAuD7XI-vo32in1yyP8m9tFs9LGRmeG5Z7gYMinMy7VUI130_provenance
a
np:Provenance
.
dgn-np:NP173581.RAuD7XI-vo32in1yyP8m9tFs9LGRmeG5Z7gYMinMy7VUI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP173581.RAuD7XI-vo32in1yyP8m9tFs9LGRmeG5Z7gYMinMy7VUI130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGN336a8077c3501654c3838eaa31422e46
sio:SIO_000628
miriam-gene:5624
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP173581.RAuD7XI-vo32in1yyP8m9tFs9LGRmeG5Z7gYMinMy7VUI130_provenance
{
dgn-np:NP173581.RAuD7XI-vo32in1yyP8m9tFs9LGRmeG5Z7gYMinMy7VUI130_assertion
dcterms:description
"[There is increasing evidence that there exist germ-line variants of the APC gene that predispose to the development of multiple colorectal adenomas and carcinoma, but without the florid phenotype of classical FAP, and possibly with importance for colorectal cancer risk in the general population.]. 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:9724771
;
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:NP173581.RAuD7XI-vo32in1yyP8m9tFs9LGRmeG5Z7gYMinMy7VUI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:34+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" .
}