Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_assertion> ?p ?o ?g. }
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- NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_assertion type Assertion NP444719.RAiv0jHJLjrYTyqETPn_phyXX5VtDCYrHnwePClhies8E130_head.
- 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.