Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_assertion> ?p ?o ?g. }
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- NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_assertion type Assertion NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_head.
- NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_assertion description "[Rett syndrome (RTT) is a neurodevelopmental disorder mostly caused by MECP2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.
- NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_assertion evidence source_evidence_literature NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.
- NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_assertion SIO_000772 24621584 NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.
- NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_assertion wasDerivedFrom befree-2016 NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.
- NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_assertion wasGeneratedBy ECO_0000203 NP1163158.RAU9dG7USvx9BdAUMwFplow2kZh2S6V6Y6IbcPkEGJ_nw130_provenance.