Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_provenance.
- NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_assertion description "[We report on a 26-month-old boy with developmental delay and multiple congenital anomalies, including many features suggestive of either branchiootorenal syndrome (BOR) or oculoauriculovertebral spectrum (OAVS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_provenance.
- NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_assertion evidence source_evidence_literature NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_provenance.
- NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_assertion SIO_000772 18666230 NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_provenance.
- NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_assertion wasDerivedFrom befree-20140225 NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_provenance.
- NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_assertion wasGeneratedBy ECO_0000203 NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP442244.RA7E-qQw3PXoeTJjgM5cqDRimRQE2fcJLhwjMzXlJFkFM130_provenance.