Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_provenance.
- NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_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." NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_provenance.
- NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_assertion evidence source_evidence_literature NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_provenance.
- NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_assertion SIO_000772 16271016 NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_provenance.
- NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_assertion wasDerivedFrom befree-20150227 NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_provenance.
- NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_assertion wasGeneratedBy ECO_0000203 NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP444289.RAEESCEzzJFrNc49ou6hW8nzZ42ga6BHRdL3vXMz07DAk130_provenance.