Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_provenance.
- NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_assertion description "[The cytogenetic study with G bands and FISH with painting for chromosome 5 and with the cri-du-chat 5p15 unique sequence probe showed a duplication and inversion of 5p [46,XX, dup(5)(p15.3 p13.3)] which overlaps with the critical region for 5p trisomy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_provenance.
- NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_assertion evidence source_evidence_literature NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_provenance.
- NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_assertion SIO_000772 16001443 NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_provenance.
- NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_assertion wasDerivedFrom befree-20140225 NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_provenance.
- NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_assertion wasGeneratedBy ECO_0000203 NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP581683.RAcJHXY30W1oLoKa8wIz8NfODaMIKk3R3sOUfyKZqTvcc130_provenance.