Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_assertion> ?p ?o ?g. }
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- NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_assertion type Assertion NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_head.
- NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_assertion description "[Following the recent discovery that the methyl-CpG binding protein 2 (MECP2) gene located on Xq28 is involved in Rett syndrome (RTT), a wild spectrum of phenotypes, including mental handicap, has been shown to be associated with mutations in MECP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.
- NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_assertion evidence source_evidence_literature NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.
- NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_assertion SIO_000772 11309367 NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.
- NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_assertion wasDerivedFrom befree-2016 NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.
- NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_assertion wasGeneratedBy ECO_0000203 NP314932.RA2ju4jnmDuavWCoH2OiS_ePz0mkdzTZLNW-MrCsogZ2k130_provenance.