Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP319915.RAANvGFQ2m3VAtOj7tDTcnLkxdnvoVaNLkTCUxYLYh2Bc130_provenance.
- 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.