Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP54321.RA2yTevgA7bTWCi1Cy0dqWrUO5G0eAwQk1F5767yqP-FE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP54321.RA2yTevgA7bTWCi1Cy0dqWrUO5G0eAwQk1F5767yqP-FE130_assertion type Assertion NP54321.RA2yTevgA7bTWCi1Cy0dqWrUO5G0eAwQk1F5767yqP-FE130_head.
- NP54321.RA2yTevgA7bTWCi1Cy0dqWrUO5G0eAwQk1F5767yqP-FE130_assertion description "[Charcot-Marie-Tooth disease (CMT) is a genetically heterogeneous disorder that has been associated with alterations of several proteins: peripheral myelin protein 22, myelin protein zero, connexin 32, early growth response factor 2, periaxin, myotubularin related protein 2, N-myc downstream regulated gene 1 product, neurofilament light chain, and kinesin 1B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54321.RA2yTevgA7bTWCi1Cy0dqWrUO5G0eAwQk1F5767yqP-FE130_provenance.
- NP54321.RA2yTevgA7bTWCi1Cy0dqWrUO5G0eAwQk1F5767yqP-FE130_assertion evidence source_evidence_literature NP54321.RA2yTevgA7bTWCi1Cy0dqWrUO5G0eAwQk1F5767yqP-FE130_provenance.
- NP54321.RA2yTevgA7bTWCi1Cy0dqWrUO5G0eAwQk1F5767yqP-FE130_assertion SIO_000772 11835375 NP54321.RA2yTevgA7bTWCi1Cy0dqWrUO5G0eAwQk1F5767yqP-FE130_provenance.
- NP54321.RA2yTevgA7bTWCi1Cy0dqWrUO5G0eAwQk1F5767yqP-FE130_assertion wasDerivedFrom gad-20130706 NP54321.RA2yTevgA7bTWCi1Cy0dqWrUO5G0eAwQk1F5767yqP-FE130_provenance.
- NP54321.RA2yTevgA7bTWCi1Cy0dqWrUO5G0eAwQk1F5767yqP-FE130_assertion wasGeneratedBy ECO_0000203 NP54321.RA2yTevgA7bTWCi1Cy0dqWrUO5G0eAwQk1F5767yqP-FE130_provenance.