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- NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_assertion type Assertion NP873179.RAoV9ZyARmIdZwmVKvNxL1HF_qBNBP9S4ziFUOy6wDjxA130_head.
- 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.