Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_assertion> ?p ?o ?g. }
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- NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_assertion type Assertion NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_head.
- NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_assertion wasGeneratedBy ECO_0000203 NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_provenance.
- NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_assertion wasDerivedFrom befree-2016 NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_provenance.
- NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_assertion SIO_000772 9615224 NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_provenance.
- NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_assertion evidence source_evidence_literature NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_provenance.
- NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_provenance.