Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_assertion> ?p ?o ?g. }
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- NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_assertion type Assertion NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_head.
- NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_assertion wasGeneratedBy ECO_0000203 NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_provenance.
- NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_assertion wasDerivedFrom befree-20140225 NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_provenance.
- NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_assertion SIO_000772 18499664 NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_provenance.
- NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_assertion evidence source_evidence_literature NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_provenance.
- NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877720.RAYML4tBWRfyerhlArCApPcADdvD1RU4bBVX_8Y6h3iOs130_provenance.