Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_assertion> ?p ?o ?g. }
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- NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_assertion type Assertion NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_head.
- NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_assertion wasGeneratedBy ECO_0000203 NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_provenance.
- NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_assertion wasDerivedFrom befree-20150227 NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_provenance.
- NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_assertion SIO_000772 24398087 NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_provenance.
- NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_assertion evidence source_evidence_literature NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_provenance.
- NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_assertion description "[Collagen type IV related nephropathies are due to the defects in collagen IV genes COL4A3, COL4A4, or COL4A5 and comprise a spectrum of phenotypes ranging from Alport Syndrome (AS) to its mild variants, termed as familial haematuria or thin basement membrane nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_provenance.