Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_provenance.
- befree-2016 importedOn "2016-02-19" NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_provenance.
- NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_assertion wasGeneratedBy ECO_0000203 NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_provenance.
- NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_assertion wasDerivedFrom befree-2016 NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_provenance.
- NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_assertion SIO_000772 19100507 NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_provenance.
- NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_assertion evidence source_evidence_literature NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_provenance.
- NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_assertion description "[Trisomy 12 was seen in 12 (15.2%) cases, and was followed by 17p13.1 (TP53) deletions and 11q22.3 (ATM) deletions in 6 (7.6%) and 4 (5.1%) patients, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710592.RAazGxB7veUaeT-mAIWzJMlRRyzJDo20UCF5Jq6Y0L0sU130_provenance.