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- NP1851.RARWz2J3_CNXC1ubAGLtaGxYn4Jznk9ov5RDJIyYIjJfU130_assertion type Assertion NP1851.RARWz2J3_CNXC1ubAGLtaGxYn4Jznk9ov5RDJIyYIjJfU130_head.
- NP1851.RARWz2J3_CNXC1ubAGLtaGxYn4Jznk9ov5RDJIyYIjJfU130_assertion wasGeneratedBy ECO_0000218 NP1851.RARWz2J3_CNXC1ubAGLtaGxYn4Jznk9ov5RDJIyYIjJfU130_provenance.
- NP1851.RARWz2J3_CNXC1ubAGLtaGxYn4Jznk9ov5RDJIyYIjJfU130_assertion wasDerivedFrom uniprot-2016 NP1851.RARWz2J3_CNXC1ubAGLtaGxYn4Jznk9ov5RDJIyYIjJfU130_provenance.
- NP1851.RARWz2J3_CNXC1ubAGLtaGxYn4Jznk9ov5RDJIyYIjJfU130_assertion SIO_000772 11826022 NP1851.RARWz2J3_CNXC1ubAGLtaGxYn4Jznk9ov5RDJIyYIjJfU130_provenance.
- NP1851.RARWz2J3_CNXC1ubAGLtaGxYn4Jznk9ov5RDJIyYIjJfU130_assertion evidence source_evidence_curated NP1851.RARWz2J3_CNXC1ubAGLtaGxYn4Jznk9ov5RDJIyYIjJfU130_provenance.
- NP1851.RARWz2J3_CNXC1ubAGLtaGxYn4Jznk9ov5RDJIyYIjJfU130_assertion description "[These results indicate that CSGE is highly sensitive for the detection of mutations in FBN1, and that molecular diagnostics is a useful means of confirming clinical diagnoses of MFS and related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1851.RARWz2J3_CNXC1ubAGLtaGxYn4Jznk9ov5RDJIyYIjJfU130_provenance.