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- source_evidence_literature type ECO_0000212 NP270355.RAH68C87LqOvF1NfdistaaHgQf-ohOJKgvCtBVpxwRB1c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP270355.RAH68C87LqOvF1NfdistaaHgQf-ohOJKgvCtBVpxwRB1c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP270355.RAH68C87LqOvF1NfdistaaHgQf-ohOJKgvCtBVpxwRB1c130_provenance.
- NP270355.RAH68C87LqOvF1NfdistaaHgQf-ohOJKgvCtBVpxwRB1c130_assertion description "[Patients with BPES carrying larger deletions encompassing FOXL2 present more frequently with associated clinical findings, such as mental retardation (D?haene et al., 2009).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270355.RAH68C87LqOvF1NfdistaaHgQf-ohOJKgvCtBVpxwRB1c130_provenance.
- NP270355.RAH68C87LqOvF1NfdistaaHgQf-ohOJKgvCtBVpxwRB1c130_assertion evidence source_evidence_literature NP270355.RAH68C87LqOvF1NfdistaaHgQf-ohOJKgvCtBVpxwRB1c130_provenance.
- NP270355.RAH68C87LqOvF1NfdistaaHgQf-ohOJKgvCtBVpxwRB1c130_assertion SIO_000772 21934608 NP270355.RAH68C87LqOvF1NfdistaaHgQf-ohOJKgvCtBVpxwRB1c130_provenance.
- NP270355.RAH68C87LqOvF1NfdistaaHgQf-ohOJKgvCtBVpxwRB1c130_assertion wasDerivedFrom befree-20150227 NP270355.RAH68C87LqOvF1NfdistaaHgQf-ohOJKgvCtBVpxwRB1c130_provenance.
- NP270355.RAH68C87LqOvF1NfdistaaHgQf-ohOJKgvCtBVpxwRB1c130_assertion wasGeneratedBy ECO_0000203 NP270355.RAH68C87LqOvF1NfdistaaHgQf-ohOJKgvCtBVpxwRB1c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP270355.RAH68C87LqOvF1NfdistaaHgQf-ohOJKgvCtBVpxwRB1c130_provenance.