@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE
> .
@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/v4.0.0/void/
> .
dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_head
{
this:
np:hasAssertion
dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_assertion
;
np:hasProvenance
dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_provenance
;
np:hasPublicationInfo
dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_assertion
a
np:Assertion
.
dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_provenance
a
np:Provenance
.
dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0001430
a
ncit:C7057
.
dgn-gda:DGN83c261957d8368d457d66b459e088384
sio:SIO_000628
miriam-gene:324
,
lld:C0001430
;
a
sio:SIO_001121
.
}
dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_provenance
{
dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_assertion
dcterms:description
"[Based on the association of APC missense variants with multiple adenomas, we proposed that much of this may be due to the cumulative effects of low frequency, low penetrance variants, and the rare variant hypothesis.]. 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:16596323
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:51+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}