Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1211773.RANyojRkOc9rIlffl1diHfbkGyyz02JwQV0IrGeTysehY130_provenance.