Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_provenance.
- NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_assertion wasGeneratedBy ECO_0000203 NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_provenance.
- NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_assertion wasDerivedFrom befree-20150227 NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_provenance.
- NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_assertion SIO_000772 23161389 NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_provenance.
- NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_assertion evidence source_evidence_literature NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_provenance.
- NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_assertion description "[Typical HPFH is associated with promoter mutations or large deletions affecting the human fetal globin (HBG1 and HBG2) genes, while genetic defects in other genes involved in human erythropoiesis, e.g.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_provenance.