Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_provenance.
- NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_assertion description "[Overall, we found 9 (13.8%) large genomic deletions or duplications: 7 out of 45 CRC patients with family history and 2 out of 20 young CRC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_provenance.
- NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_assertion evidence source_evidence_literature NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_provenance.
- NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_assertion SIO_000772 15949572 NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_provenance.
- NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_assertion wasDerivedFrom befree-2016 NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_provenance.
- NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_assertion wasGeneratedBy ECO_0000203 NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_provenance.
- befree-2016 importedOn "2016-02-19" NP498924.RAlhdhvyjo4EXZcMq96w4_AXNnaR1VUKcO8a4zToRsAIU130_provenance.