Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP884570.RAXbWSGQOnc6eIWa0eHn60bEYiXg-9EI90rDFNDox3kvs130_assertion> ?p ?o ?g. }
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- NP884570.RAXbWSGQOnc6eIWa0eHn60bEYiXg-9EI90rDFNDox3kvs130_assertion type Assertion NP884570.RAXbWSGQOnc6eIWa0eHn60bEYiXg-9EI90rDFNDox3kvs130_head.
- NP884570.RAXbWSGQOnc6eIWa0eHn60bEYiXg-9EI90rDFNDox3kvs130_assertion wasGeneratedBy ECO_0000203 NP884570.RAXbWSGQOnc6eIWa0eHn60bEYiXg-9EI90rDFNDox3kvs130_provenance.
- NP884570.RAXbWSGQOnc6eIWa0eHn60bEYiXg-9EI90rDFNDox3kvs130_assertion wasDerivedFrom befree-20140225 NP884570.RAXbWSGQOnc6eIWa0eHn60bEYiXg-9EI90rDFNDox3kvs130_provenance.
- NP884570.RAXbWSGQOnc6eIWa0eHn60bEYiXg-9EI90rDFNDox3kvs130_assertion SIO_000772 17855451 NP884570.RAXbWSGQOnc6eIWa0eHn60bEYiXg-9EI90rDFNDox3kvs130_provenance.
- NP884570.RAXbWSGQOnc6eIWa0eHn60bEYiXg-9EI90rDFNDox3kvs130_assertion evidence source_evidence_literature NP884570.RAXbWSGQOnc6eIWa0eHn60bEYiXg-9EI90rDFNDox3kvs130_provenance.
- NP884570.RAXbWSGQOnc6eIWa0eHn60bEYiXg-9EI90rDFNDox3kvs130_assertion description "[However, the first mutation reported to cause PCWH was a disruption of the native stop codon that by conceptual translation extends the protein into the 3' untranslated region (3'-UTR) for an additional 82 residues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP884570.RAXbWSGQOnc6eIWa0eHn60bEYiXg-9EI90rDFNDox3kvs130_provenance.