@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP202310.RAUYyEq99l39MSt4RFyJtiAKh8zaEL5HAlJKc0c7I92zY
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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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:NP202310.RAUYyEq99l39MSt4RFyJtiAKh8zaEL5HAlJKc0c7I92zY130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP202310.RAUYyEq99l39MSt4RFyJtiAKh8zaEL5HAlJKc0c7I92zY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP202310.RAUYyEq99l39MSt4RFyJtiAKh8zaEL5HAlJKc0c7I92zY130_assertion
a
np:Assertion
.
dgn-np:NP202310.RAUYyEq99l39MSt4RFyJtiAKh8zaEL5HAlJKc0c7I92zY130_provenance
a
np:Provenance
.
dgn-np:NP202310.RAUYyEq99l39MSt4RFyJtiAKh8zaEL5HAlJKc0c7I92zY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP202310.RAUYyEq99l39MSt4RFyJtiAKh8zaEL5HAlJKc0c7I92zY130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN37b23798a6981057a6e7e5cefa7e7cca
sio:SIO_000628
miriam-gene:5624
,
lld:C1527249
;
a
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.
}
dgn-np:NP202310.RAUYyEq99l39MSt4RFyJtiAKh8zaEL5HAlJKc0c7I92zY130_provenance
{
dgn-np:NP202310.RAUYyEq99l39MSt4RFyJtiAKh8zaEL5HAlJKc0c7I92zY130_assertion
dcterms:description
"[This is an 11-year survey of molecular analysis of APC germline mutations for the province of Quebec done at the Molecular Pathology Unit of the Jewish General Hospital which offers genetic testing for hereditary forms of colorectal cancer for the whole of Quebec province.]. 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:21779980
;
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:NP202310.RAUYyEq99l39MSt4RFyJtiAKh8zaEL5HAlJKc0c7I92zY130_publicationInfo
{
this:
dcterms:created
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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
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<
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> , <
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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pav:version
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