Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP826376.RAC6r9Rf8yb5334VZzrD--LaGI5JgoSA7FTilo0VDhSmw130_assertion> ?p ?o ?g. }
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- NP826376.RAC6r9Rf8yb5334VZzrD--LaGI5JgoSA7FTilo0VDhSmw130_assertion type Assertion NP826376.RAC6r9Rf8yb5334VZzrD--LaGI5JgoSA7FTilo0VDhSmw130_head.
- NP826376.RAC6r9Rf8yb5334VZzrD--LaGI5JgoSA7FTilo0VDhSmw130_assertion wasGeneratedBy ECO_0000203 NP826376.RAC6r9Rf8yb5334VZzrD--LaGI5JgoSA7FTilo0VDhSmw130_provenance.
- NP826376.RAC6r9Rf8yb5334VZzrD--LaGI5JgoSA7FTilo0VDhSmw130_assertion wasDerivedFrom befree-2016 NP826376.RAC6r9Rf8yb5334VZzrD--LaGI5JgoSA7FTilo0VDhSmw130_provenance.
- NP826376.RAC6r9Rf8yb5334VZzrD--LaGI5JgoSA7FTilo0VDhSmw130_assertion SIO_000772 20633900 NP826376.RAC6r9Rf8yb5334VZzrD--LaGI5JgoSA7FTilo0VDhSmw130_provenance.
- NP826376.RAC6r9Rf8yb5334VZzrD--LaGI5JgoSA7FTilo0VDhSmw130_assertion evidence source_evidence_literature NP826376.RAC6r9Rf8yb5334VZzrD--LaGI5JgoSA7FTilo0VDhSmw130_provenance.
- NP826376.RAC6r9Rf8yb5334VZzrD--LaGI5JgoSA7FTilo0VDhSmw130_assertion description "[A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: phenotypic spectrum and structural study of FHL1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP826376.RAC6r9Rf8yb5334VZzrD--LaGI5JgoSA7FTilo0VDhSmw130_provenance.