Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP873251.RAcVtG6xI1_IHl7voXBYl2wU3uRy0Zm4jVDJsOse_Pc00130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP873251.RAcVtG6xI1_IHl7voXBYl2wU3uRy0Zm4jVDJsOse_Pc00130_assertion type Assertion NP873251.RAcVtG6xI1_IHl7voXBYl2wU3uRy0Zm4jVDJsOse_Pc00130_head.
- NP873251.RAcVtG6xI1_IHl7voXBYl2wU3uRy0Zm4jVDJsOse_Pc00130_assertion description "[Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873251.RAcVtG6xI1_IHl7voXBYl2wU3uRy0Zm4jVDJsOse_Pc00130_provenance.
- NP873251.RAcVtG6xI1_IHl7voXBYl2wU3uRy0Zm4jVDJsOse_Pc00130_assertion evidence source_evidence_literature NP873251.RAcVtG6xI1_IHl7voXBYl2wU3uRy0Zm4jVDJsOse_Pc00130_provenance.
- NP873251.RAcVtG6xI1_IHl7voXBYl2wU3uRy0Zm4jVDJsOse_Pc00130_assertion SIO_000772 23793026 NP873251.RAcVtG6xI1_IHl7voXBYl2wU3uRy0Zm4jVDJsOse_Pc00130_provenance.
- NP873251.RAcVtG6xI1_IHl7voXBYl2wU3uRy0Zm4jVDJsOse_Pc00130_assertion wasDerivedFrom befree-20150227 NP873251.RAcVtG6xI1_IHl7voXBYl2wU3uRy0Zm4jVDJsOse_Pc00130_provenance.
- NP873251.RAcVtG6xI1_IHl7voXBYl2wU3uRy0Zm4jVDJsOse_Pc00130_assertion wasGeneratedBy ECO_0000203 NP873251.RAcVtG6xI1_IHl7voXBYl2wU3uRy0Zm4jVDJsOse_Pc00130_provenance.