Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_provenance.
- NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_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." NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_provenance.
- NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_assertion evidence source_evidence_literature NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_provenance.
- NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_assertion SIO_000772 22078000 NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_provenance.
- NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_assertion wasDerivedFrom befree-20150227 NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_provenance.
- NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_assertion wasGeneratedBy ECO_0000203 NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788397.RAmEQPQfjhHyE27lqb_kOqnA2vMNOvVIhKW3Fm8OIJEvs130_provenance.