Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP184639.RAeA9CrK8C6jvWbQCYqqvKMMnPoXNyH219shf30lAhi-4130_assertion> ?p ?o ?g. }
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- NP184639.RAeA9CrK8C6jvWbQCYqqvKMMnPoXNyH219shf30lAhi-4130_assertion type Assertion NP184639.RAeA9CrK8C6jvWbQCYqqvKMMnPoXNyH219shf30lAhi-4130_head.
- NP184639.RAeA9CrK8C6jvWbQCYqqvKMMnPoXNyH219shf30lAhi-4130_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." NP184639.RAeA9CrK8C6jvWbQCYqqvKMMnPoXNyH219shf30lAhi-4130_provenance.
- NP184639.RAeA9CrK8C6jvWbQCYqqvKMMnPoXNyH219shf30lAhi-4130_assertion evidence source_evidence_literature NP184639.RAeA9CrK8C6jvWbQCYqqvKMMnPoXNyH219shf30lAhi-4130_provenance.
- NP184639.RAeA9CrK8C6jvWbQCYqqvKMMnPoXNyH219shf30lAhi-4130_assertion SIO_000772 21705420 NP184639.RAeA9CrK8C6jvWbQCYqqvKMMnPoXNyH219shf30lAhi-4130_provenance.
- NP184639.RAeA9CrK8C6jvWbQCYqqvKMMnPoXNyH219shf30lAhi-4130_assertion wasDerivedFrom befree-20140225 NP184639.RAeA9CrK8C6jvWbQCYqqvKMMnPoXNyH219shf30lAhi-4130_provenance.
- NP184639.RAeA9CrK8C6jvWbQCYqqvKMMnPoXNyH219shf30lAhi-4130_assertion wasGeneratedBy ECO_0000203 NP184639.RAeA9CrK8C6jvWbQCYqqvKMMnPoXNyH219shf30lAhi-4130_provenance.