Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP344398.RAV1GW5aUk-8yyM6r8V51_3FHKt2Qbg1-UScEbtDLR8h4130_assertion> ?p ?o ?g. }
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- NP344398.RAV1GW5aUk-8yyM6r8V51_3FHKt2Qbg1-UScEbtDLR8h4130_assertion type Assertion NP344398.RAV1GW5aUk-8yyM6r8V51_3FHKt2Qbg1-UScEbtDLR8h4130_head.
- NP344398.RAV1GW5aUk-8yyM6r8V51_3FHKt2Qbg1-UScEbtDLR8h4130_assertion description "[Charcot-Marie-Tooth disease (CMT) is a genetically heterogeneous disorder that has been associated with alterations of several proteins: peripheral myelin protein 22, myelin protein zero, connexin 32, early growth response factor 2, periaxin, myotubularin related protein 2, N-myc downstream regulated gene 1 product, neurofilament light chain, and kinesin 1B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP344398.RAV1GW5aUk-8yyM6r8V51_3FHKt2Qbg1-UScEbtDLR8h4130_provenance.
- NP344398.RAV1GW5aUk-8yyM6r8V51_3FHKt2Qbg1-UScEbtDLR8h4130_assertion evidence source_evidence_literature NP344398.RAV1GW5aUk-8yyM6r8V51_3FHKt2Qbg1-UScEbtDLR8h4130_provenance.
- NP344398.RAV1GW5aUk-8yyM6r8V51_3FHKt2Qbg1-UScEbtDLR8h4130_assertion SIO_000772 11835375 NP344398.RAV1GW5aUk-8yyM6r8V51_3FHKt2Qbg1-UScEbtDLR8h4130_provenance.
- NP344398.RAV1GW5aUk-8yyM6r8V51_3FHKt2Qbg1-UScEbtDLR8h4130_assertion wasDerivedFrom befree-2016 NP344398.RAV1GW5aUk-8yyM6r8V51_3FHKt2Qbg1-UScEbtDLR8h4130_provenance.
- NP344398.RAV1GW5aUk-8yyM6r8V51_3FHKt2Qbg1-UScEbtDLR8h4130_assertion wasGeneratedBy ECO_0000203 NP344398.RAV1GW5aUk-8yyM6r8V51_3FHKt2Qbg1-UScEbtDLR8h4130_provenance.