Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP860633.RAp3bxDMnVS0yC6iWwBgt1hek01OvAETiq411hNOhU6W4130_assertion> ?p ?o ?g. }
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- NP860633.RAp3bxDMnVS0yC6iWwBgt1hek01OvAETiq411hNOhU6W4130_assertion type Assertion NP860633.RAp3bxDMnVS0yC6iWwBgt1hek01OvAETiq411hNOhU6W4130_head.
- NP860633.RAp3bxDMnVS0yC6iWwBgt1hek01OvAETiq411hNOhU6W4130_assertion description "[Patients in whom no mutation is identified through this mutation protocol, may be sub-cohorts representing a different FAP pathogenesis including MYH associated polyposis and somatic cell mosaicism for APC gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860633.RAp3bxDMnVS0yC6iWwBgt1hek01OvAETiq411hNOhU6W4130_provenance.
- NP860633.RAp3bxDMnVS0yC6iWwBgt1hek01OvAETiq411hNOhU6W4130_assertion evidence source_evidence_literature NP860633.RAp3bxDMnVS0yC6iWwBgt1hek01OvAETiq411hNOhU6W4130_provenance.
- NP860633.RAp3bxDMnVS0yC6iWwBgt1hek01OvAETiq411hNOhU6W4130_assertion SIO_000772 19414146 NP860633.RAp3bxDMnVS0yC6iWwBgt1hek01OvAETiq411hNOhU6W4130_provenance.
- NP860633.RAp3bxDMnVS0yC6iWwBgt1hek01OvAETiq411hNOhU6W4130_assertion wasDerivedFrom befree-20150227 NP860633.RAp3bxDMnVS0yC6iWwBgt1hek01OvAETiq411hNOhU6W4130_provenance.
- NP860633.RAp3bxDMnVS0yC6iWwBgt1hek01OvAETiq411hNOhU6W4130_assertion wasGeneratedBy ECO_0000203 NP860633.RAp3bxDMnVS0yC6iWwBgt1hek01OvAETiq411hNOhU6W4130_provenance.