Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_provenance.
- NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_assertion description "[Many of the mutations known to cause either syndromic or nonsyndromic deafness occur in genes that interact with actin (e.g., the myosins, espin, and harmonin).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_provenance.
- NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_assertion evidence source_evidence_literature NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_provenance.
- NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_assertion SIO_000772 13680526 NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_provenance.
- NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_assertion wasDerivedFrom befree-20150227 NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_provenance.
- NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_assertion wasGeneratedBy ECO_0000203 NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP953445.RAjpg7LgaIw_SthW45ddABnt0giPknHqEj7xVCnkFrT0k130_provenance.