Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_provenance.
- 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.
- uniprot-2016 importedOn "2016-01-25" NP3308.RAa369vao-B2OjjGyLN5gOR57k3zsmTgo_gcQSUNGOv3c130_provenance.