Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP540691.RArgsJj7XBNAtUXM924bJEHTPu8gsCoxkKrwMcmzCuv5o130_assertion> ?p ?o ?g. }
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- NP540691.RArgsJj7XBNAtUXM924bJEHTPu8gsCoxkKrwMcmzCuv5o130_assertion type Assertion NP540691.RArgsJj7XBNAtUXM924bJEHTPu8gsCoxkKrwMcmzCuv5o130_head.
- NP540691.RArgsJj7XBNAtUXM924bJEHTPu8gsCoxkKrwMcmzCuv5o130_assertion description "[Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540691.RArgsJj7XBNAtUXM924bJEHTPu8gsCoxkKrwMcmzCuv5o130_provenance.
- NP540691.RArgsJj7XBNAtUXM924bJEHTPu8gsCoxkKrwMcmzCuv5o130_assertion evidence source_evidence_literature NP540691.RArgsJj7XBNAtUXM924bJEHTPu8gsCoxkKrwMcmzCuv5o130_provenance.
- NP540691.RArgsJj7XBNAtUXM924bJEHTPu8gsCoxkKrwMcmzCuv5o130_assertion SIO_000772 16542389 NP540691.RArgsJj7XBNAtUXM924bJEHTPu8gsCoxkKrwMcmzCuv5o130_provenance.
- NP540691.RArgsJj7XBNAtUXM924bJEHTPu8gsCoxkKrwMcmzCuv5o130_assertion wasDerivedFrom befree-2016 NP540691.RArgsJj7XBNAtUXM924bJEHTPu8gsCoxkKrwMcmzCuv5o130_provenance.
- NP540691.RArgsJj7XBNAtUXM924bJEHTPu8gsCoxkKrwMcmzCuv5o130_assertion wasGeneratedBy ECO_0000203 NP540691.RArgsJj7XBNAtUXM924bJEHTPu8gsCoxkKrwMcmzCuv5o130_provenance.