Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_provenance.
- NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_assertion description "[The absence of del(5q), trisomy 8 and 21, as well as the rarity of monosomy 7, contrasts with pooled published data and may reflect our exclusion of closely related disorders, in particular MDS with fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_provenance.
- NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_assertion evidence source_evidence_literature NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_provenance.
- NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_assertion SIO_000772 7819070 NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_provenance.
- NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_assertion wasDerivedFrom befree-20150227 NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_provenance.
- NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_assertion wasGeneratedBy ECO_0000203 NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_provenance.