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- source_evidence_literature type ECO_0000212 NP605856.RA31dJfP-FGriBpQuEyger-YYd7h4-BddRgTuecRU8hqY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605856.RA31dJfP-FGriBpQuEyger-YYd7h4-BddRgTuecRU8hqY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605856.RA31dJfP-FGriBpQuEyger-YYd7h4-BddRgTuecRU8hqY130_provenance.
- NP605856.RA31dJfP-FGriBpQuEyger-YYd7h4-BddRgTuecRU8hqY130_assertion description "[We conclude that the 5q-syndrome may be best defined as primary MDS of the FAB type RA with a 5q deletion as the sole karyotypic abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP605856.RA31dJfP-FGriBpQuEyger-YYd7h4-BddRgTuecRU8hqY130_provenance.
- NP605856.RA31dJfP-FGriBpQuEyger-YYd7h4-BddRgTuecRU8hqY130_assertion evidence source_evidence_literature NP605856.RA31dJfP-FGriBpQuEyger-YYd7h4-BddRgTuecRU8hqY130_provenance.
- NP605856.RA31dJfP-FGriBpQuEyger-YYd7h4-BddRgTuecRU8hqY130_assertion SIO_000772 7604812 NP605856.RA31dJfP-FGriBpQuEyger-YYd7h4-BddRgTuecRU8hqY130_provenance.
- NP605856.RA31dJfP-FGriBpQuEyger-YYd7h4-BddRgTuecRU8hqY130_assertion wasDerivedFrom befree-20150227 NP605856.RA31dJfP-FGriBpQuEyger-YYd7h4-BddRgTuecRU8hqY130_provenance.
- NP605856.RA31dJfP-FGriBpQuEyger-YYd7h4-BddRgTuecRU8hqY130_assertion wasGeneratedBy ECO_0000203 NP605856.RA31dJfP-FGriBpQuEyger-YYd7h4-BddRgTuecRU8hqY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP605856.RA31dJfP-FGriBpQuEyger-YYd7h4-BddRgTuecRU8hqY130_provenance.