Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_assertion> ?p ?o ?g. }
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- NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_assertion type Assertion NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_head.
- NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_assertion wasGeneratedBy ECO_0000203 NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_provenance.
- NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_assertion wasDerivedFrom befree-2016 NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_provenance.
- NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_assertion SIO_000772 17387578 NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_provenance.
- NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_assertion evidence source_evidence_literature NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_provenance.
- NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_assertion description "[Rett syndrome (RTT), an X-linked dominant neurodevelopmental disorder in females, is caused mainly by de novo mutations in the methyl-CpG-binding protein 2 gene (MECP2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601051.RAA_3o9M8enF7sfA1pZDQ_WgdX8AI_2-Svcw956OAU91U130_provenance.