Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP925747.RAREOAX2h_0pRXtHMlrVtABD91jAhP_LhWm1st2PnjFtg130_assertion> ?p ?o ?g. }
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- NP925747.RAREOAX2h_0pRXtHMlrVtABD91jAhP_LhWm1st2PnjFtg130_assertion type Assertion NP925747.RAREOAX2h_0pRXtHMlrVtABD91jAhP_LhWm1st2PnjFtg130_head.
- NP925747.RAREOAX2h_0pRXtHMlrVtABD91jAhP_LhWm1st2PnjFtg130_assertion description "[A novel MPZ mutation in Charcot-Marie-Tooth disease type 1B with focally folded myelin and multiple entrapment neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925747.RAREOAX2h_0pRXtHMlrVtABD91jAhP_LhWm1st2PnjFtg130_provenance.
- NP925747.RAREOAX2h_0pRXtHMlrVtABD91jAhP_LhWm1st2PnjFtg130_assertion evidence source_evidence_literature NP925747.RAREOAX2h_0pRXtHMlrVtABD91jAhP_LhWm1st2PnjFtg130_provenance.
- NP925747.RAREOAX2h_0pRXtHMlrVtABD91jAhP_LhWm1st2PnjFtg130_assertion SIO_000772 21940171 NP925747.RAREOAX2h_0pRXtHMlrVtABD91jAhP_LhWm1st2PnjFtg130_provenance.
- NP925747.RAREOAX2h_0pRXtHMlrVtABD91jAhP_LhWm1st2PnjFtg130_assertion wasDerivedFrom befree-2016 NP925747.RAREOAX2h_0pRXtHMlrVtABD91jAhP_LhWm1st2PnjFtg130_provenance.
- NP925747.RAREOAX2h_0pRXtHMlrVtABD91jAhP_LhWm1st2PnjFtg130_assertion wasGeneratedBy ECO_0000203 NP925747.RAREOAX2h_0pRXtHMlrVtABD91jAhP_LhWm1st2PnjFtg130_provenance.