Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_provenance.
- NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_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." NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_provenance.
- NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_assertion evidence source_evidence_literature NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_provenance.
- NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_assertion SIO_000772 21796726 NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_provenance.
- NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_assertion wasDerivedFrom befree-20150227 NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_provenance.
- NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_assertion wasGeneratedBy ECO_0000203 NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP810970.RAkmyB6liPZDKVLc-DwtMkbLw15DzaCtIMcJ46EYaLrU8130_provenance.