Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_provenance.
- NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_assertion wasGeneratedBy ECO_0000203 NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_provenance.
- NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_assertion wasDerivedFrom befree-20150227 NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_provenance.
- NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_assertion SIO_000772 17434305 NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_provenance.
- NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_assertion evidence source_evidence_literature NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_provenance.
- NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_assertion description "[Mutations in embryonic MyHC (MYH3) and perinatal MyHC (MYH8), which are myosin isoforms expressed during muscle development, are associated with distal arthrogryposis syndromes with no or minor muscle weakness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583441.RArM7bGrVawFjm51V2e0T3PsVtp_zxGc9aDpaIRt59n9Y130_provenance.