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- NP1367753.RAeGg27TqzVjbqJjCE5-cRfmtQ7-0Ljv_jrR3PmYVFzfk130_assertion type Assertion NP1367753.RAeGg27TqzVjbqJjCE5-cRfmtQ7-0Ljv_jrR3PmYVFzfk130_head.
- NP1367753.RAeGg27TqzVjbqJjCE5-cRfmtQ7-0Ljv_jrR3PmYVFzfk130_assertion description "[A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1367753.RAeGg27TqzVjbqJjCE5-cRfmtQ7-0Ljv_jrR3PmYVFzfk130_provenance.
- NP1367753.RAeGg27TqzVjbqJjCE5-cRfmtQ7-0Ljv_jrR3PmYVFzfk130_assertion evidence source_evidence_literature NP1367753.RAeGg27TqzVjbqJjCE5-cRfmtQ7-0Ljv_jrR3PmYVFzfk130_provenance.
- NP1367753.RAeGg27TqzVjbqJjCE5-cRfmtQ7-0Ljv_jrR3PmYVFzfk130_assertion SIO_000772 9040737 NP1367753.RAeGg27TqzVjbqJjCE5-cRfmtQ7-0Ljv_jrR3PmYVFzfk130_provenance.
- NP1367753.RAeGg27TqzVjbqJjCE5-cRfmtQ7-0Ljv_jrR3PmYVFzfk130_assertion wasDerivedFrom befree-2016 NP1367753.RAeGg27TqzVjbqJjCE5-cRfmtQ7-0Ljv_jrR3PmYVFzfk130_provenance.
- NP1367753.RAeGg27TqzVjbqJjCE5-cRfmtQ7-0Ljv_jrR3PmYVFzfk130_assertion wasGeneratedBy ECO_0000203 NP1367753.RAeGg27TqzVjbqJjCE5-cRfmtQ7-0Ljv_jrR3PmYVFzfk130_provenance.