Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_provenance.
- NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_assertion description "[The nature of the mutation has been considered the major determinant of the phenotype within this group that comprises the otopalatodigital syndromes (OPD1, OPD2) and Melnick-Needles syndrome besides FMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_provenance.
- NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_assertion evidence source_evidence_curated NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_provenance.
- NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_assertion SIO_000772 16596676 NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_provenance.
- NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_assertion wasDerivedFrom ctd_human-20130708 NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_provenance.
- NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_assertion wasGeneratedBy ECO_0000218 NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP15933.RA0NZmkMzsUjusl0iC-a-WejGPlfPsS0zvFLwnMKOVeNM130_provenance.