Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_provenance.
- NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_assertion description "[Y272 is most likely critical for SMN(T) function as it is a target for recurring mutations and is associated with type I SMA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_provenance.
- NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_assertion evidence source_evidence_literature NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_provenance.
- NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_assertion SIO_000772 10732817 NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_provenance.
- NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_assertion wasDerivedFrom befree-2016 NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_provenance.
- NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_assertion wasGeneratedBy ECO_0000203 NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_provenance.
- befree-2016 importedOn "2016-02-19" NP278936.RAz9bbOc_o8wLzLfxwW-jAnatVPEbqrKAKVOc9cNRcdFg130_provenance.