Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP938234.RAhSJEUvWqBcabScqLQz_0jPdzLjAqH74yNrRXvTtCiME130_provenance.