Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_provenance.
- NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_assertion description "[Hereditary persistence of fetal hemoglobin (HPFH) is a benign condition caused by the failure of normal switching from the fetal to the adult beta-globin gene, resulting in continuous production of fetal hemoglobin beyond the perinatal period.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_provenance.
- NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_assertion evidence source_evidence_literature NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_provenance.
- NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_assertion SIO_000772 16271016 NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_provenance.
- NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_assertion wasDerivedFrom befree-2016 NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_provenance.
- NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_assertion wasGeneratedBy ECO_0000203 NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_provenance.
- befree-2016 importedOn "2016-02-19" NP521105.RArL07c6Ieb5WCg5Fly9WmbJ4rZKI_RRsvAfx6jSuPLi0130_provenance.