Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1155669.RARVPRhRgKyyhyURq8JstG4SWgDXg60I_GnaqooHXTB3k130_assertion> ?p ?o ?g. }
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- NP1155669.RARVPRhRgKyyhyURq8JstG4SWgDXg60I_GnaqooHXTB3k130_assertion type Assertion NP1155669.RARVPRhRgKyyhyURq8JstG4SWgDXg60I_GnaqooHXTB3k130_head.
- NP1155669.RARVPRhRgKyyhyURq8JstG4SWgDXg60I_GnaqooHXTB3k130_assertion description "[The incidence of PMD with PLP1 mutations was estimated to be 1.45 per 100,000 male live births and that for congenital hypomyelinating disorders with unknown cause to be 0.41 per 100,000 live births.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1155669.RARVPRhRgKyyhyURq8JstG4SWgDXg60I_GnaqooHXTB3k130_provenance.
- NP1155669.RARVPRhRgKyyhyURq8JstG4SWgDXg60I_GnaqooHXTB3k130_assertion evidence source_evidence_literature NP1155669.RARVPRhRgKyyhyURq8JstG4SWgDXg60I_GnaqooHXTB3k130_provenance.
- NP1155669.RARVPRhRgKyyhyURq8JstG4SWgDXg60I_GnaqooHXTB3k130_assertion SIO_000772 24532200 NP1155669.RARVPRhRgKyyhyURq8JstG4SWgDXg60I_GnaqooHXTB3k130_provenance.
- NP1155669.RARVPRhRgKyyhyURq8JstG4SWgDXg60I_GnaqooHXTB3k130_assertion wasDerivedFrom befree-2016 NP1155669.RARVPRhRgKyyhyURq8JstG4SWgDXg60I_GnaqooHXTB3k130_provenance.
- NP1155669.RARVPRhRgKyyhyURq8JstG4SWgDXg60I_GnaqooHXTB3k130_assertion wasGeneratedBy ECO_0000203 NP1155669.RARVPRhRgKyyhyURq8JstG4SWgDXg60I_GnaqooHXTB3k130_provenance.