Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_provenance.
- NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_assertion description "[Our findings show that functional analysis of rare missense mutations can provide a mechanistic insight into the pathogenesis of MDS and the physiological role of ?-sarcoglycan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_provenance.
- NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_assertion evidence source_evidence_literature NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_provenance.
- NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_assertion SIO_000772 21796726 NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_provenance.
- NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_assertion wasDerivedFrom befree-2016 NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_provenance.
- NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_assertion wasGeneratedBy ECO_0000203 NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_provenance.
- befree-2016 importedOn "2016-02-19" NP913000.RAjc6LJ6xtWY_NLOqxNm4p22hgKL3B5VvWGbyCoPMsAQY130_provenance.