Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_assertion> ?p ?o ?g. }
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- NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_assertion type Assertion NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_head.
- NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_assertion description "[Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_provenance.
- NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_assertion evidence source_evidence_curated NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_provenance.
- NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_assertion SIO_000772 15009458 NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_provenance.
- NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_assertion wasDerivedFrom uniprot-2016 NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_provenance.
- NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_assertion wasGeneratedBy ECO_0000218 NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_provenance.