Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_provenance.
- NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_assertion description "[COL4A5-associated X-linked Alport syndrome in a female patient with early inner ear deafness due to a mutation in MYH9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_provenance.
- NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_assertion evidence source_evidence_literature NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_provenance.
- NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_assertion SIO_000772 23144074 NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_provenance.
- NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_assertion wasDerivedFrom befree-20150227 NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_provenance.
- NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_assertion wasGeneratedBy ECO_0000203 NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583663.RAdsn9WwyDUTMzMzVSjn8stYDIUAqmV1nVQcpGNspy7Ng130_provenance.