Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_provenance.
- NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_assertion description "[The Greek form of hereditary persistence of fetal hemoglobin (HPFH) is associated with a point mutation immediately upstream of the distal of the two CCAAT elements of the A gamma-globin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_provenance.
- NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_assertion evidence source_evidence_literature NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_provenance.
- NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_assertion SIO_000772 3181130 NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_provenance.
- NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_assertion wasDerivedFrom befree-20140225 NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_provenance.
- NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_assertion wasGeneratedBy ECO_0000203 NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP264638.RAQh5LvxRd1BxX362Vtlh38F2ciB7dN8oIT7MKVJ2RK-8130_provenance.