@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP754263.RAqu2EvW9oyUtAvDx3j8dnWg1QjbEAXJpd6JDfxPceQ7A
> .
@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/v3.0.0/void/
> .
dgn-np:NP754263.RAqu2EvW9oyUtAvDx3j8dnWg1QjbEAXJpd6JDfxPceQ7A130_head
{
this:
np:hasAssertion
dgn-np:NP754263.RAqu2EvW9oyUtAvDx3j8dnWg1QjbEAXJpd6JDfxPceQ7A130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP754263.RAqu2EvW9oyUtAvDx3j8dnWg1QjbEAXJpd6JDfxPceQ7A130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP754263.RAqu2EvW9oyUtAvDx3j8dnWg1QjbEAXJpd6JDfxPceQ7A130_assertion
a
np:Assertion
.
dgn-np:NP754263.RAqu2EvW9oyUtAvDx3j8dnWg1QjbEAXJpd6JDfxPceQ7A130_provenance
a
np:Provenance
.
dgn-np:NP754263.RAqu2EvW9oyUtAvDx3j8dnWg1QjbEAXJpd6JDfxPceQ7A130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP754263.RAqu2EvW9oyUtAvDx3j8dnWg1QjbEAXJpd6JDfxPceQ7A130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGNf9ca29b329ebac8ef517576fca5c2fad
sio:SIO_000628
miriam-gene:7157
,
lld:C1333990
;
a
sio:SIO_001122
.
}
dgn-np:NP754263.RAqu2EvW9oyUtAvDx3j8dnWg1QjbEAXJpd6JDfxPceQ7A130_provenance
{
dgn-np:NP754263.RAqu2EvW9oyUtAvDx3j8dnWg1QjbEAXJpd6JDfxPceQ7A130_assertion
dcterms:description
"[We have previously reported that the common, functionally different variants Arg72Pro in p53 and Arg462Gln in RNASEL are associated with the age of disease onset of colorectal cancer in Lynch syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:17224235
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP754263.RAqu2EvW9oyUtAvDx3j8dnWg1QjbEAXJpd6JDfxPceQ7A130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
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> , <
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
"v3.0.0.0" .
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pav:version
"v3.0.0" .
}