Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_provenance.
- NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_assertion description "[Our result suggests an important role for homozygous c.558C>A mutations in the UGT1A1 gene in the development of severe unconjugated hyperbilirubinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_provenance.
- NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_assertion evidence source_evidence_literature NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_provenance.
- NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_assertion SIO_000772 25729974 NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_provenance.
- NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_assertion wasDerivedFrom befree-2016 NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_provenance.
- NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_assertion wasGeneratedBy ECO_0000203 NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1267358.RAIOEw1xqaUzYDhxYBxP6JyrYfztP0FW4zHcxRwjZAlK8130_provenance.