@prefix this: <
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> .
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> .
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@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
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> .
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http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
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> .
@prefix wi: <
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> .
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> .
@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/
> .
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http://rdf.disgenet.org/v4.0.0/void/
> .
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a
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miriam-gene:860
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN047ca084457e391a0987c6ccaf8e9d3f
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.
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dgn-np:NP853302.RAdbOvrILhf6UysLfTEqAvg3tt55uQG50yMGJy8ue99oI130_assertion
dcterms:description
"[We evaluated genetic variation in RUNX1 (40 tagSNPs), RUNX2 (19 tagSNPs), RUNX3 (9 tagSNPs), MAPK1 (6 tagSNPs), eIF4E (3 tagSNPs), eIF4EBP2 (2 tagSNP) and eIF4EBP3 (2 tagSNPs) to determine associations with colorectal cancer (CRC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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miriam-pubmed:21088106
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pav:importedOn
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xsd:date
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dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
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dgn-np:NP853302.RAdbOvrILhf6UysLfTEqAvg3tt55uQG50yMGJy8ue99oI130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
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> , <
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