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- source_evidence_literature type ECO_0000212 NP924053.RApqZAuGuJhM11r9dz0-eihlEXDgFDlGhfvoud-Pj9YvI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924053.RApqZAuGuJhM11r9dz0-eihlEXDgFDlGhfvoud-Pj9YvI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924053.RApqZAuGuJhM11r9dz0-eihlEXDgFDlGhfvoud-Pj9YvI130_provenance.
- NP924053.RApqZAuGuJhM11r9dz0-eihlEXDgFDlGhfvoud-Pj9YvI130_assertion description "[The human hereditary disease Acatalasia (AC) is characterized by low or no catalase activity in all body tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924053.RApqZAuGuJhM11r9dz0-eihlEXDgFDlGhfvoud-Pj9YvI130_provenance.
- NP924053.RApqZAuGuJhM11r9dz0-eihlEXDgFDlGhfvoud-Pj9YvI130_assertion evidence source_evidence_literature NP924053.RApqZAuGuJhM11r9dz0-eihlEXDgFDlGhfvoud-Pj9YvI130_provenance.
- NP924053.RApqZAuGuJhM11r9dz0-eihlEXDgFDlGhfvoud-Pj9YvI130_assertion SIO_000772 3377795 NP924053.RApqZAuGuJhM11r9dz0-eihlEXDgFDlGhfvoud-Pj9YvI130_provenance.
- NP924053.RApqZAuGuJhM11r9dz0-eihlEXDgFDlGhfvoud-Pj9YvI130_assertion wasDerivedFrom befree-20140225 NP924053.RApqZAuGuJhM11r9dz0-eihlEXDgFDlGhfvoud-Pj9YvI130_provenance.
- NP924053.RApqZAuGuJhM11r9dz0-eihlEXDgFDlGhfvoud-Pj9YvI130_assertion wasGeneratedBy ECO_0000203 NP924053.RApqZAuGuJhM11r9dz0-eihlEXDgFDlGhfvoud-Pj9YvI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP924053.RApqZAuGuJhM11r9dz0-eihlEXDgFDlGhfvoud-Pj9YvI130_provenance.