Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_assertion> ?p ?o ?g. }
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- NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_assertion type Assertion NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_head.
- NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_assertion description "[IGS is caused by specific malabsorption of cobalamin (Cbl) due to bi-allelic mutations in either the cubilin gene (CUBN) or the human amnionless homolog (AMN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_provenance.
- NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_assertion evidence source_evidence_literature NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_provenance.
- NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_assertion SIO_000772 22078000 NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_provenance.
- NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_assertion wasDerivedFrom befree-2016 NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_provenance.
- NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_assertion wasGeneratedBy ECO_0000203 NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_provenance.