Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3629.RAtmKy6W-mGC-0EsHWS9NeXwRprv-ZpZsIwRM-hP3rxlo130_assertion> ?p ?o ?g. }
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- NP3629.RAtmKy6W-mGC-0EsHWS9NeXwRprv-ZpZsIwRM-hP3rxlo130_assertion type Assertion NP3629.RAtmKy6W-mGC-0EsHWS9NeXwRprv-ZpZsIwRM-hP3rxlo130_head.
- NP3629.RAtmKy6W-mGC-0EsHWS9NeXwRprv-ZpZsIwRM-hP3rxlo130_assertion wasGeneratedBy ECO_0000218 NP3629.RAtmKy6W-mGC-0EsHWS9NeXwRprv-ZpZsIwRM-hP3rxlo130_provenance.
- NP3629.RAtmKy6W-mGC-0EsHWS9NeXwRprv-ZpZsIwRM-hP3rxlo130_assertion wasDerivedFrom uniprot-20130724 NP3629.RAtmKy6W-mGC-0EsHWS9NeXwRprv-ZpZsIwRM-hP3rxlo130_provenance.
- NP3629.RAtmKy6W-mGC-0EsHWS9NeXwRprv-ZpZsIwRM-hP3rxlo130_assertion SIO_000772 11531804 NP3629.RAtmKy6W-mGC-0EsHWS9NeXwRprv-ZpZsIwRM-hP3rxlo130_provenance.
- NP3629.RAtmKy6W-mGC-0EsHWS9NeXwRprv-ZpZsIwRM-hP3rxlo130_assertion evidence source_evidence_curated NP3629.RAtmKy6W-mGC-0EsHWS9NeXwRprv-ZpZsIwRM-hP3rxlo130_provenance.
- NP3629.RAtmKy6W-mGC-0EsHWS9NeXwRprv-ZpZsIwRM-hP3rxlo130_assertion description "[New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3629.RAtmKy6W-mGC-0EsHWS9NeXwRprv-ZpZsIwRM-hP3rxlo130_provenance.