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- NP886158.RAaeYZPYp0PnrEyrgVidJahnZBpCrhvVDx-4hnRJhUCT8130_assertion type Assertion NP886158.RAaeYZPYp0PnrEyrgVidJahnZBpCrhvVDx-4hnRJhUCT8130_head.
- NP886158.RAaeYZPYp0PnrEyrgVidJahnZBpCrhvVDx-4hnRJhUCT8130_assertion wasGeneratedBy ECO_0000203 NP886158.RAaeYZPYp0PnrEyrgVidJahnZBpCrhvVDx-4hnRJhUCT8130_provenance.
- NP886158.RAaeYZPYp0PnrEyrgVidJahnZBpCrhvVDx-4hnRJhUCT8130_assertion wasDerivedFrom befree-20140225 NP886158.RAaeYZPYp0PnrEyrgVidJahnZBpCrhvVDx-4hnRJhUCT8130_provenance.
- NP886158.RAaeYZPYp0PnrEyrgVidJahnZBpCrhvVDx-4hnRJhUCT8130_assertion SIO_000772 20578134 NP886158.RAaeYZPYp0PnrEyrgVidJahnZBpCrhvVDx-4hnRJhUCT8130_provenance.
- NP886158.RAaeYZPYp0PnrEyrgVidJahnZBpCrhvVDx-4hnRJhUCT8130_assertion evidence source_evidence_literature NP886158.RAaeYZPYp0PnrEyrgVidJahnZBpCrhvVDx-4hnRJhUCT8130_provenance.
- NP886158.RAaeYZPYp0PnrEyrgVidJahnZBpCrhvVDx-4hnRJhUCT8130_assertion description "[Microdeletions of the 21q22.11q22.12 region encompassing the RUNX1 gene have been reported in nine patients presenting with syndromic thrombocytopenia and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886158.RAaeYZPYp0PnrEyrgVidJahnZBpCrhvVDx-4hnRJhUCT8130_provenance.