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- NP1126825.RAo86hPQKMxgmaw0mBkKmGFSjJLpAftEMB6HpZL1NmEYk130_assertion type Assertion NP1126825.RAo86hPQKMxgmaw0mBkKmGFSjJLpAftEMB6HpZL1NmEYk130_head.
- NP1126825.RAo86hPQKMxgmaw0mBkKmGFSjJLpAftEMB6HpZL1NmEYk130_assertion description "[Mutations in FBN1, ADAMTS10, or ADAMTS17 cause Weill-Marchesani syndrome by disrupting the microfibrillar environment, while geleophysic dysplasia is associated with enhanced TGF-? signaling mediated through mutations in FBN1 or ADAMTSL2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1126825.RAo86hPQKMxgmaw0mBkKmGFSjJLpAftEMB6HpZL1NmEYk130_provenance.
- NP1126825.RAo86hPQKMxgmaw0mBkKmGFSjJLpAftEMB6HpZL1NmEYk130_assertion evidence source_evidence_literature NP1126825.RAo86hPQKMxgmaw0mBkKmGFSjJLpAftEMB6HpZL1NmEYk130_provenance.
- NP1126825.RAo86hPQKMxgmaw0mBkKmGFSjJLpAftEMB6HpZL1NmEYk130_assertion SIO_000772 24214363 NP1126825.RAo86hPQKMxgmaw0mBkKmGFSjJLpAftEMB6HpZL1NmEYk130_provenance.
- NP1126825.RAo86hPQKMxgmaw0mBkKmGFSjJLpAftEMB6HpZL1NmEYk130_assertion wasDerivedFrom befree-2016 NP1126825.RAo86hPQKMxgmaw0mBkKmGFSjJLpAftEMB6HpZL1NmEYk130_provenance.
- NP1126825.RAo86hPQKMxgmaw0mBkKmGFSjJLpAftEMB6HpZL1NmEYk130_assertion wasGeneratedBy ECO_0000203 NP1126825.RAo86hPQKMxgmaw0mBkKmGFSjJLpAftEMB6HpZL1NmEYk130_provenance.