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- NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_assertion type Assertion NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_head.
- NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_assertion description "[These new data further support ASXL1 as cause of BOS and may contribute to a more precise definition of the phenotype caused by the disruption of this gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance.
- NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_assertion evidence source_evidence_literature NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance.
- NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_assertion SIO_000772 22419483 NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance.
- NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_assertion wasDerivedFrom befree-2016 NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance.
- NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_assertion wasGeneratedBy ECO_0000203 NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance.