Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_assertion> ?p ?o ?g. }
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- NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_assertion type Assertion NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_head.
- NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_assertion description "[Four missense mutations, CFH p.V837I, p.Y1058H, p.V1060L and THBD p.R403K may predispose to aHUS manifestation; the remaining seven missense mutations were likely neutral.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_provenance.
- NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_assertion evidence source_evidence_literature NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_provenance.
- NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_assertion SIO_000772 25135378 NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_provenance.
- NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_assertion wasDerivedFrom befree-2016 NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_provenance.
- NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_assertion wasGeneratedBy ECO_0000203 NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_provenance.