Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_assertion> ?p ?o ?g. }
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- NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_assertion type Assertion NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_head.
- NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_assertion description "[Hereditary thrombocythemia is a rare autosomal dominant disorder caused by mutations in either the thrombopoietin gene (TPO) or its receptor c-MPL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_provenance.
- NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_assertion evidence source_evidence_literature NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_provenance.
- NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_assertion SIO_000772 19553636 NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_provenance.
- NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_assertion wasDerivedFrom befree-2016 NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_provenance.
- NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_assertion wasGeneratedBy ECO_0000203 NP747384.RAUYCyZYcR8gf6oEx8Ce1SGBlSZq_hHonar6MhYiX8L0k130_provenance.