Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP915829.RAw6sNmpf7SNF3j8PJGxyU38kk0toKcXL789CN5fr9H5c130_assertion> ?p ?o ?g. }
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- NP915829.RAw6sNmpf7SNF3j8PJGxyU38kk0toKcXL789CN5fr9H5c130_assertion type Assertion NP915829.RAw6sNmpf7SNF3j8PJGxyU38kk0toKcXL789CN5fr9H5c130_head.
- NP915829.RAw6sNmpf7SNF3j8PJGxyU38kk0toKcXL789CN5fr9H5c130_assertion wasGeneratedBy ECO_0000203 NP915829.RAw6sNmpf7SNF3j8PJGxyU38kk0toKcXL789CN5fr9H5c130_provenance.
- NP915829.RAw6sNmpf7SNF3j8PJGxyU38kk0toKcXL789CN5fr9H5c130_assertion wasDerivedFrom befree-20140225 NP915829.RAw6sNmpf7SNF3j8PJGxyU38kk0toKcXL789CN5fr9H5c130_provenance.
- NP915829.RAw6sNmpf7SNF3j8PJGxyU38kk0toKcXL789CN5fr9H5c130_assertion SIO_000772 20660572 NP915829.RAw6sNmpf7SNF3j8PJGxyU38kk0toKcXL789CN5fr9H5c130_provenance.
- NP915829.RAw6sNmpf7SNF3j8PJGxyU38kk0toKcXL789CN5fr9H5c130_assertion evidence source_evidence_literature NP915829.RAw6sNmpf7SNF3j8PJGxyU38kk0toKcXL789CN5fr9H5c130_provenance.
- NP915829.RAw6sNmpf7SNF3j8PJGxyU38kk0toKcXL789CN5fr9H5c130_assertion description "[In the NET-Registry, 9/101 patients (8.9%) with ICTs had germline mutations, 8 in MEN1 and 1 in VHL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915829.RAw6sNmpf7SNF3j8PJGxyU38kk0toKcXL789CN5fr9H5c130_provenance.