Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP789407.RAsTmPE4gOxGjEZFd0FcQ-Lem15XI55u1GOKy1JbdDlDw130_assertion> ?p ?o ?g. }
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- NP789407.RAsTmPE4gOxGjEZFd0FcQ-Lem15XI55u1GOKy1JbdDlDw130_assertion type Assertion NP789407.RAsTmPE4gOxGjEZFd0FcQ-Lem15XI55u1GOKy1JbdDlDw130_head.
- NP789407.RAsTmPE4gOxGjEZFd0FcQ-Lem15XI55u1GOKy1JbdDlDw130_assertion wasGeneratedBy ECO_0000203 NP789407.RAsTmPE4gOxGjEZFd0FcQ-Lem15XI55u1GOKy1JbdDlDw130_provenance.
- NP789407.RAsTmPE4gOxGjEZFd0FcQ-Lem15XI55u1GOKy1JbdDlDw130_assertion wasDerivedFrom befree-20140225 NP789407.RAsTmPE4gOxGjEZFd0FcQ-Lem15XI55u1GOKy1JbdDlDw130_provenance.
- NP789407.RAsTmPE4gOxGjEZFd0FcQ-Lem15XI55u1GOKy1JbdDlDw130_assertion SIO_000772 7478198 NP789407.RAsTmPE4gOxGjEZFd0FcQ-Lem15XI55u1GOKy1JbdDlDw130_provenance.
- NP789407.RAsTmPE4gOxGjEZFd0FcQ-Lem15XI55u1GOKy1JbdDlDw130_assertion evidence source_evidence_literature NP789407.RAsTmPE4gOxGjEZFd0FcQ-Lem15XI55u1GOKy1JbdDlDw130_provenance.
- NP789407.RAsTmPE4gOxGjEZFd0FcQ-Lem15XI55u1GOKy1JbdDlDw130_assertion description "[In particular the absence of molecular changes in the PMP-22 gene definitively sets HMSN with MOs apart from the more common CMT1A, hereditary neuropathy with liability to pressure palsies (HNPP) and progressive sensory-motor polyneuropathy with tomaculous changes at sural nerve biopsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789407.RAsTmPE4gOxGjEZFd0FcQ-Lem15XI55u1GOKy1JbdDlDw130_provenance.