Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_provenance.
- NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_assertion description "[DNA analyses showed that seven (three boys, four girls) of these 20 (35%) had G6PD Aures (nt 143 T - > C), a variant associated with favism which was recently reported in an Algerian.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_provenance.
- NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_assertion evidence source_evidence_literature NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_provenance.
- NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_assertion SIO_000772 8787363 NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_provenance.
- NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_assertion wasDerivedFrom befree-20150227 NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_provenance.
- NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_assertion wasGeneratedBy ECO_0000203 NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP793407.RApZENeSvGCtVwTFp7pMYCtvoY8tKP1hAHYUnUXDjB3-M130_provenance.