Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_provenance.
- NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_assertion description "[We have analyzed a series of 35 DNA samples from patients affected with cystic fibrosis (CF), Duchenne and Becker muscular dystrophies (DMD/BMD), or sarcoglycanopathies, and have characterized exonic copy-number changes that have been validated with other methods.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_provenance.
- NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_assertion evidence source_evidence_literature NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_provenance.
- NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_assertion SIO_000772 18683213 NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_provenance.
- NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_assertion wasDerivedFrom befree-2016 NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_provenance.
- NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_assertion wasGeneratedBy ECO_0000203 NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_provenance.
- befree-2016 importedOn "2016-02-19" NP686336.RADr8eRPEjmF3wKHcqvvk4QT9qUkO0Xkz4onkSQbj6fUg130_provenance.