Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1366635.RA7qfQPDIXGrzSx3Bu4S5DJiCr1exKIFzTRcLPRoK4v5Y130_assertion> ?p ?o ?g. }
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- NP1366635.RA7qfQPDIXGrzSx3Bu4S5DJiCr1exKIFzTRcLPRoK4v5Y130_assertion type Assertion NP1366635.RA7qfQPDIXGrzSx3Bu4S5DJiCr1exKIFzTRcLPRoK4v5Y130_head.
- NP1366635.RA7qfQPDIXGrzSx3Bu4S5DJiCr1exKIFzTRcLPRoK4v5Y130_assertion description "[More recently, FBN1 has also been shown to harbor mutations related to a spectrum of conditions phenotypically related to MFS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1366635.RA7qfQPDIXGrzSx3Bu4S5DJiCr1exKIFzTRcLPRoK4v5Y130_provenance.
- NP1366635.RA7qfQPDIXGrzSx3Bu4S5DJiCr1exKIFzTRcLPRoK4v5Y130_assertion evidence source_evidence_literature NP1366635.RA7qfQPDIXGrzSx3Bu4S5DJiCr1exKIFzTRcLPRoK4v5Y130_provenance.
- NP1366635.RA7qfQPDIXGrzSx3Bu4S5DJiCr1exKIFzTRcLPRoK4v5Y130_assertion SIO_000772 9016526 NP1366635.RA7qfQPDIXGrzSx3Bu4S5DJiCr1exKIFzTRcLPRoK4v5Y130_provenance.
- NP1366635.RA7qfQPDIXGrzSx3Bu4S5DJiCr1exKIFzTRcLPRoK4v5Y130_assertion wasDerivedFrom befree-2016 NP1366635.RA7qfQPDIXGrzSx3Bu4S5DJiCr1exKIFzTRcLPRoK4v5Y130_provenance.
- NP1366635.RA7qfQPDIXGrzSx3Bu4S5DJiCr1exKIFzTRcLPRoK4v5Y130_assertion wasGeneratedBy ECO_0000203 NP1366635.RA7qfQPDIXGrzSx3Bu4S5DJiCr1exKIFzTRcLPRoK4v5Y130_provenance.