Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_provenance.
- NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_assertion description "[The homozygous frequency of GSTP1 genotype did not differ significantly between groups of ALL (3.7%), ANLL patients (9.1%) and controls (4.9%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_provenance.
- NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_assertion evidence source_evidence_literature NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_provenance.
- NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_assertion SIO_000772 12827651 NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_provenance.
- NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_assertion wasDerivedFrom befree-20140225 NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_provenance.
- NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_assertion wasGeneratedBy ECO_0000203 NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP873647.RAzQhYBGuVlQr5fIqR9j3fvaAx_Uo-URr68BXa4dBD5HA130_provenance.