@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU
> .
@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:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_head
{
this:
np:hasAssertion
dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_assertion
;
np:hasProvenance
dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_provenance
;
np:hasPublicationInfo
dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_assertion
a
np:Assertion
.
dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_provenance
a
np:Provenance
.
dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN3b16b5586208d86d1c3347d5dacbc130
sio:SIO_000628
miriam-gene:324
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_provenance
{
dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_assertion
dcterms:description
"[Germline mutations in the adenomatous polyposis coli (APC) gene cause familial adenomatous polyposis (FAP), an autosomal dominant disease characterized by hundreds to thousands of adenomatous polyps in the colon and rectum, with progression to colorectal cancer.]. 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:18406876
;
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:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:22+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" .
}