Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_provenance.
- NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_assertion description "[Rod-shaped dimers of tropomyosin regulate actin-myosin interactions and ?-tropomyosin mutations have been associated with nemaline myopathy, cap myopathy, Escobar syndrome and distal arthrogryposis types 1A and 2B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_provenance.
- NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_assertion evidence source_evidence_literature NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_provenance.
- NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_assertion SIO_000772 23413262 NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_provenance.
- NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_assertion wasDerivedFrom befree-20150227 NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_provenance.
- NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_assertion wasGeneratedBy ECO_0000203 NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP756323.RAwXm7NIdQlBg9o73JkBSkeiBKBTNXG7CdHBO_u5DgNpQ130_provenance.