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- NP320029.RAIW0oVp7tMW3BNbhKJV7Ye6lft_1MltDEAZ4vy1A8i5I130_assertion type Assertion NP320029.RAIW0oVp7tMW3BNbhKJV7Ye6lft_1MltDEAZ4vy1A8i5I130_head.
- NP320029.RAIW0oVp7tMW3BNbhKJV7Ye6lft_1MltDEAZ4vy1A8i5I130_assertion wasGeneratedBy ECO_0000203 NP320029.RAIW0oVp7tMW3BNbhKJV7Ye6lft_1MltDEAZ4vy1A8i5I130_provenance.
- NP320029.RAIW0oVp7tMW3BNbhKJV7Ye6lft_1MltDEAZ4vy1A8i5I130_assertion wasDerivedFrom befree-20150227 NP320029.RAIW0oVp7tMW3BNbhKJV7Ye6lft_1MltDEAZ4vy1A8i5I130_provenance.
- NP320029.RAIW0oVp7tMW3BNbhKJV7Ye6lft_1MltDEAZ4vy1A8i5I130_assertion SIO_000772 24398087 NP320029.RAIW0oVp7tMW3BNbhKJV7Ye6lft_1MltDEAZ4vy1A8i5I130_provenance.
- NP320029.RAIW0oVp7tMW3BNbhKJV7Ye6lft_1MltDEAZ4vy1A8i5I130_assertion evidence source_evidence_literature NP320029.RAIW0oVp7tMW3BNbhKJV7Ye6lft_1MltDEAZ4vy1A8i5I130_provenance.
- NP320029.RAIW0oVp7tMW3BNbhKJV7Ye6lft_1MltDEAZ4vy1A8i5I130_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." NP320029.RAIW0oVp7tMW3BNbhKJV7Ye6lft_1MltDEAZ4vy1A8i5I130_provenance.