Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6696.RAuRG2e1bDoQi69i4vDJIeeKzL1WtpSERP_tjdDAct5ic130_assertion> ?p ?o ?g. }
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- NP6696.RAuRG2e1bDoQi69i4vDJIeeKzL1WtpSERP_tjdDAct5ic130_assertion type Assertion NP6696.RAuRG2e1bDoQi69i4vDJIeeKzL1WtpSERP_tjdDAct5ic130_head.
- NP6696.RAuRG2e1bDoQi69i4vDJIeeKzL1WtpSERP_tjdDAct5ic130_assertion description "[Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P? phosphatase FIG4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6696.RAuRG2e1bDoQi69i4vDJIeeKzL1WtpSERP_tjdDAct5ic130_provenance.
- NP6696.RAuRG2e1bDoQi69i4vDJIeeKzL1WtpSERP_tjdDAct5ic130_assertion evidence source_evidence_curated NP6696.RAuRG2e1bDoQi69i4vDJIeeKzL1WtpSERP_tjdDAct5ic130_provenance.
- NP6696.RAuRG2e1bDoQi69i4vDJIeeKzL1WtpSERP_tjdDAct5ic130_assertion SIO_000772 21705420 NP6696.RAuRG2e1bDoQi69i4vDJIeeKzL1WtpSERP_tjdDAct5ic130_provenance.
- NP6696.RAuRG2e1bDoQi69i4vDJIeeKzL1WtpSERP_tjdDAct5ic130_assertion wasDerivedFrom uniprot-2016 NP6696.RAuRG2e1bDoQi69i4vDJIeeKzL1WtpSERP_tjdDAct5ic130_provenance.
- NP6696.RAuRG2e1bDoQi69i4vDJIeeKzL1WtpSERP_tjdDAct5ic130_assertion wasGeneratedBy ECO_0000218 NP6696.RAuRG2e1bDoQi69i4vDJIeeKzL1WtpSERP_tjdDAct5ic130_provenance.