@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI
> .
@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 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:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_head
{
this:
np:hasAssertion
dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_assertion
;
np:hasProvenance
dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_provenance
;
np:hasPublicationInfo
dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_assertion
a
np:Assertion
.
dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_provenance
a
np:Provenance
.
dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN04a5139f22fd2db4c206575b92f96298
sio:SIO_000628
miriam-gene:595
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_provenance
{
dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_assertion
dct:description
"[Polymorphisms in the 2 cell-cycle control genes Aurora A and Cyclin D1 have previously been associated with changes in the age of onset of colorectal cancer in persons harboring germline mutations in DNA mismatch repair genes associated with hereditary nonpolyposis colorectal cancer (HNPCC).]. 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:18027856
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:21+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}