Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_provenance.
- befree-2016 importedOn "2016-02-19" NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_provenance.
- NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_assertion wasGeneratedBy ECO_0000203 NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_provenance.
- NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_assertion wasDerivedFrom befree-2016 NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_provenance.
- NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_assertion SIO_000772 19181095 NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_provenance.
- NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_assertion evidence source_evidence_literature NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_provenance.
- NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_assertion description "[Mutations in embryonic MyHC (MYH3) and perinatal MyHC (MYH8) 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." NP717519.RAtUHUSpjJzh7e5WutUCTWNbglXwoIh4MCNzfY5mvWt1o130_provenance.