Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_assertion> ?p ?o ?g. }
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- NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_assertion type Assertion NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_head.
- NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_assertion wasGeneratedBy ECO_0000203 NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.
- NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_assertion wasDerivedFrom befree-20140225 NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.
- NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_assertion SIO_000772 15776429 NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.
- NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_assertion evidence source_evidence_literature NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.
- NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_assertion description "[Recently, SIMPLE/LITAF was shown to be responsible for an autosomal dominant demyelinating form of CMT linked to 16p (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP241737.RA1N07fFp3FwHqVsEtfTJkn_x5tZvGxFUNyPeDMZqnTqY130_provenance.