Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_assertion> ?p ?o ?g. }
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- NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_assertion type Assertion NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_head.
- NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_assertion description "[An earlier study has shown that FAP patients with mutations in codons 136-302 of the APC gene do not develop congenital hypertrophy of the retinal pigment epithelium (CHRPE), whereas those with mutations in codons 463-1387 regularly do.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_provenance.
- NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_assertion evidence source_evidence_literature NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_provenance.
- NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_assertion SIO_000772 7795585 NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_provenance.
- NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_assertion wasDerivedFrom befree-2016 NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_provenance.
- NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_assertion wasGeneratedBy ECO_0000203 NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_provenance.