Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP831745.RAmLWZ4dCfspawCAwjFI6DbaCZ2zr7RvhftmfqIv9RnaI130_assertion> ?p ?o ?g. }
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- NP831745.RAmLWZ4dCfspawCAwjFI6DbaCZ2zr7RvhftmfqIv9RnaI130_assertion type Assertion NP831745.RAmLWZ4dCfspawCAwjFI6DbaCZ2zr7RvhftmfqIv9RnaI130_head.
- NP831745.RAmLWZ4dCfspawCAwjFI6DbaCZ2zr7RvhftmfqIv9RnaI130_assertion description "[Alport syndrome (ATS) is a type-IV collagen inherited disorder, caused by mutations in COL4A3 and COL4A4 (autosomal recessive) or COL4A5 (X-linked).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831745.RAmLWZ4dCfspawCAwjFI6DbaCZ2zr7RvhftmfqIv9RnaI130_provenance.
- NP831745.RAmLWZ4dCfspawCAwjFI6DbaCZ2zr7RvhftmfqIv9RnaI130_assertion evidence source_evidence_literature NP831745.RAmLWZ4dCfspawCAwjFI6DbaCZ2zr7RvhftmfqIv9RnaI130_provenance.
- NP831745.RAmLWZ4dCfspawCAwjFI6DbaCZ2zr7RvhftmfqIv9RnaI130_assertion SIO_000772 23144074 NP831745.RAmLWZ4dCfspawCAwjFI6DbaCZ2zr7RvhftmfqIv9RnaI130_provenance.
- NP831745.RAmLWZ4dCfspawCAwjFI6DbaCZ2zr7RvhftmfqIv9RnaI130_assertion wasDerivedFrom befree-20140225 NP831745.RAmLWZ4dCfspawCAwjFI6DbaCZ2zr7RvhftmfqIv9RnaI130_provenance.
- NP831745.RAmLWZ4dCfspawCAwjFI6DbaCZ2zr7RvhftmfqIv9RnaI130_assertion wasGeneratedBy ECO_0000203 NP831745.RAmLWZ4dCfspawCAwjFI6DbaCZ2zr7RvhftmfqIv9RnaI130_provenance.