Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_provenance.
- NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_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." NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_provenance.
- NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_assertion evidence source_evidence_literature NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_provenance.
- NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_assertion SIO_000772 23144074 NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_provenance.
- NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_assertion wasDerivedFrom befree-20150227 NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_provenance.
- NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_assertion wasGeneratedBy ECO_0000203 NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP320162.RAl9xv8bIJD9_uYfqD4TtMZpDtH3LLpTCUU5XM2VrUEIo130_provenance.