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- source_evidence_literature type ECO_0000212 NP781585.RA0GhLoeLdPebUCkXHo9Xt7hM56O6g-Zu4SGwE8N991GU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781585.RA0GhLoeLdPebUCkXHo9Xt7hM56O6g-Zu4SGwE8N991GU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781585.RA0GhLoeLdPebUCkXHo9Xt7hM56O6g-Zu4SGwE8N991GU130_provenance.
- NP781585.RA0GhLoeLdPebUCkXHo9Xt7hM56O6g-Zu4SGwE8N991GU130_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." NP781585.RA0GhLoeLdPebUCkXHo9Xt7hM56O6g-Zu4SGwE8N991GU130_provenance.
- NP781585.RA0GhLoeLdPebUCkXHo9Xt7hM56O6g-Zu4SGwE8N991GU130_assertion evidence source_evidence_literature NP781585.RA0GhLoeLdPebUCkXHo9Xt7hM56O6g-Zu4SGwE8N991GU130_provenance.
- NP781585.RA0GhLoeLdPebUCkXHo9Xt7hM56O6g-Zu4SGwE8N991GU130_assertion SIO_000772 7604812 NP781585.RA0GhLoeLdPebUCkXHo9Xt7hM56O6g-Zu4SGwE8N991GU130_provenance.
- NP781585.RA0GhLoeLdPebUCkXHo9Xt7hM56O6g-Zu4SGwE8N991GU130_assertion wasDerivedFrom befree-20150227 NP781585.RA0GhLoeLdPebUCkXHo9Xt7hM56O6g-Zu4SGwE8N991GU130_provenance.
- NP781585.RA0GhLoeLdPebUCkXHo9Xt7hM56O6g-Zu4SGwE8N991GU130_assertion wasGeneratedBy ECO_0000203 NP781585.RA0GhLoeLdPebUCkXHo9Xt7hM56O6g-Zu4SGwE8N991GU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781585.RA0GhLoeLdPebUCkXHo9Xt7hM56O6g-Zu4SGwE8N991GU130_provenance.