Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_assertion> ?p ?o ?g. }
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- NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_assertion type Assertion NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_head.
- NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_assertion description "[We performed direct genotyping of INF2 in 16 index patients with Charcot-Marie-Tooth neuropathy and FSGS who did not have a mutation in PMP22 or MPZ, encoding peripheral myelin protein 22 and myelin protein zero, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_provenance.
- NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_assertion evidence source_evidence_literature NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_provenance.
- NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_assertion SIO_000772 22187985 NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_provenance.
- NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_assertion wasDerivedFrom befree-2016 NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_provenance.
- NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_assertion wasGeneratedBy ECO_0000203 NP948365.RAddb-4g5az7lkWw1fxYytevnQPAXD1obt8r6prhv7evw130_provenance.