Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_provenance.
- NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_assertion description "[To determine whether glucose-6-phosphate dehydrogenase (G6PD), uridine-diphosphoglucuronosyltransferase 1A1 (UGT1A1), and hepatic solute carrier organic anion transporter 1B1 (SLCO1B1) gene variants occur at greater frequency in neonates with significant hyperbilirubinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_provenance.
- NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_assertion evidence source_evidence_literature NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_provenance.
- NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_assertion SIO_000772 19858149 NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_provenance.
- NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_assertion wasDerivedFrom befree-2016 NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_provenance.
- NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_assertion wasGeneratedBy ECO_0000203 NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_provenance.
- befree-2016 importedOn "2016-02-19" NP771801.RAFXEaHgqxKgvLbApIpudhXrL5Dnd_sOCUBcQIBwINkBA130_provenance.