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- NP201539.RAso7j2GitQ8_kQECnWUa9khwegWm7s6JLUMUBlC1X918130_assertion type Assertion NP201539.RAso7j2GitQ8_kQECnWUa9khwegWm7s6JLUMUBlC1X918130_head.
- NP201539.RAso7j2GitQ8_kQECnWUa9khwegWm7s6JLUMUBlC1X918130_assertion description "[Interstitial deletion of 11(p11.2p12): a newly described contiguous gene deletion syndrome involving the gene for hereditary multiple exostoses (EXT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201539.RAso7j2GitQ8_kQECnWUa9khwegWm7s6JLUMUBlC1X918130_provenance.
- NP201539.RAso7j2GitQ8_kQECnWUa9khwegWm7s6JLUMUBlC1X918130_assertion evidence source_evidence_literature NP201539.RAso7j2GitQ8_kQECnWUa9khwegWm7s6JLUMUBlC1X918130_provenance.
- NP201539.RAso7j2GitQ8_kQECnWUa9khwegWm7s6JLUMUBlC1X918130_assertion SIO_000772 8882796 NP201539.RAso7j2GitQ8_kQECnWUa9khwegWm7s6JLUMUBlC1X918130_provenance.
- NP201539.RAso7j2GitQ8_kQECnWUa9khwegWm7s6JLUMUBlC1X918130_assertion wasDerivedFrom befree-20140225 NP201539.RAso7j2GitQ8_kQECnWUa9khwegWm7s6JLUMUBlC1X918130_provenance.
- NP201539.RAso7j2GitQ8_kQECnWUa9khwegWm7s6JLUMUBlC1X918130_assertion wasGeneratedBy ECO_0000203 NP201539.RAso7j2GitQ8_kQECnWUa9khwegWm7s6JLUMUBlC1X918130_provenance.