Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP617646.RAyAaTtJ_rJSq1_zmO-cDintiZ5VsWsqPxAiqKUC1lOYo130_assertion> ?p ?o ?g. }
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- NP617646.RAyAaTtJ_rJSq1_zmO-cDintiZ5VsWsqPxAiqKUC1lOYo130_assertion type Assertion NP617646.RAyAaTtJ_rJSq1_zmO-cDintiZ5VsWsqPxAiqKUC1lOYo130_head.
- NP617646.RAyAaTtJ_rJSq1_zmO-cDintiZ5VsWsqPxAiqKUC1lOYo130_assertion description "[Hereditary sensory neuropathy type I (HSN I) is an axonal form of autosomal-dominant hereditary motor and sensory neuropathy distinguished by prominent sensory loss that leads to painless injuries.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP617646.RAyAaTtJ_rJSq1_zmO-cDintiZ5VsWsqPxAiqKUC1lOYo130_provenance.
- NP617646.RAyAaTtJ_rJSq1_zmO-cDintiZ5VsWsqPxAiqKUC1lOYo130_assertion evidence source_evidence_literature NP617646.RAyAaTtJ_rJSq1_zmO-cDintiZ5VsWsqPxAiqKUC1lOYo130_provenance.
- NP617646.RAyAaTtJ_rJSq1_zmO-cDintiZ5VsWsqPxAiqKUC1lOYo130_assertion SIO_000772 21194679 NP617646.RAyAaTtJ_rJSq1_zmO-cDintiZ5VsWsqPxAiqKUC1lOYo130_provenance.
- NP617646.RAyAaTtJ_rJSq1_zmO-cDintiZ5VsWsqPxAiqKUC1lOYo130_assertion wasDerivedFrom befree-20140225 NP617646.RAyAaTtJ_rJSq1_zmO-cDintiZ5VsWsqPxAiqKUC1lOYo130_provenance.
- NP617646.RAyAaTtJ_rJSq1_zmO-cDintiZ5VsWsqPxAiqKUC1lOYo130_assertion wasGeneratedBy ECO_0000203 NP617646.RAyAaTtJ_rJSq1_zmO-cDintiZ5VsWsqPxAiqKUC1lOYo130_provenance.