Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_provenance.
- NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_assertion description "[p94 (calpain3), a muscle-specific member of the calpain family, has been shown to be responsible for limb-girdle muscular dystrophy type 2A (LGMD2A), a form of autosomal recessive and progressive neuromuscular disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_provenance.
- NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_assertion evidence source_evidence_literature NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_provenance.
- NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_assertion SIO_000772 9642272 NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_provenance.
- NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_assertion wasDerivedFrom befree-2016 NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_provenance.
- NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_assertion wasGeneratedBy ECO_0000203 NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1398197.RA6wUsMbwRbYggw3ON6-MW6AbjSMhd2wg2EwAToZv3vsU130_provenance.