Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_assertion> ?p ?o ?g. }
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- NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_assertion type Assertion NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_head.
- NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_assertion description "[These results demonstrate the importance of ACVRL1 and ENG mutations in German hereditary hemorrhagic telangiectasia (HHT) patients displaying mutation frequencies over 80%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_provenance.
- NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_assertion evidence source_evidence_literature NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_provenance.
- NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_assertion SIO_000772 15880681 NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_provenance.
- NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_assertion wasDerivedFrom lhgdn-20090331 NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_provenance.
- NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_assertion wasGeneratedBy ECO_0000203 NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_provenance.