Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP761582.RAF8XcnoIuggY-JrEI0Xogyh1_Euc5XccDk6tUc-U3tM0130_assertion> ?p ?o ?g. }
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- NP761582.RAF8XcnoIuggY-JrEI0Xogyh1_Euc5XccDk6tUc-U3tM0130_assertion type Assertion NP761582.RAF8XcnoIuggY-JrEI0Xogyh1_Euc5XccDk6tUc-U3tM0130_head.
- NP761582.RAF8XcnoIuggY-JrEI0Xogyh1_Euc5XccDk6tUc-U3tM0130_assertion description "[Charcot-Marie-Tooth disease comprises a heterogeneous group of hereditary neuropathies which fall into two main groups: demyelinating CMT1 with reduced nerve conduction velocity and axonal CMT2 with normal nerve conduction velocity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761582.RAF8XcnoIuggY-JrEI0Xogyh1_Euc5XccDk6tUc-U3tM0130_provenance.
- NP761582.RAF8XcnoIuggY-JrEI0Xogyh1_Euc5XccDk6tUc-U3tM0130_assertion evidence source_evidence_literature NP761582.RAF8XcnoIuggY-JrEI0Xogyh1_Euc5XccDk6tUc-U3tM0130_provenance.
- NP761582.RAF8XcnoIuggY-JrEI0Xogyh1_Euc5XccDk6tUc-U3tM0130_assertion SIO_000772 14733962 NP761582.RAF8XcnoIuggY-JrEI0Xogyh1_Euc5XccDk6tUc-U3tM0130_provenance.
- NP761582.RAF8XcnoIuggY-JrEI0Xogyh1_Euc5XccDk6tUc-U3tM0130_assertion wasDerivedFrom befree-20140225 NP761582.RAF8XcnoIuggY-JrEI0Xogyh1_Euc5XccDk6tUc-U3tM0130_provenance.
- NP761582.RAF8XcnoIuggY-JrEI0Xogyh1_Euc5XccDk6tUc-U3tM0130_assertion wasGeneratedBy ECO_0000203 NP761582.RAF8XcnoIuggY-JrEI0Xogyh1_Euc5XccDk6tUc-U3tM0130_provenance.