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- NP869499.RAi6K6e_zf5ZFnbwRu0FI6LyIa8Grzg59zdP9AnJOUee4130_assertion type Assertion NP869499.RAi6K6e_zf5ZFnbwRu0FI6LyIa8Grzg59zdP9AnJOUee4130_head.
- NP869499.RAi6K6e_zf5ZFnbwRu0FI6LyIa8Grzg59zdP9AnJOUee4130_assertion wasGeneratedBy ECO_0000203 NP869499.RAi6K6e_zf5ZFnbwRu0FI6LyIa8Grzg59zdP9AnJOUee4130_provenance.
- NP869499.RAi6K6e_zf5ZFnbwRu0FI6LyIa8Grzg59zdP9AnJOUee4130_assertion wasDerivedFrom befree-20140225 NP869499.RAi6K6e_zf5ZFnbwRu0FI6LyIa8Grzg59zdP9AnJOUee4130_provenance.
- NP869499.RAi6K6e_zf5ZFnbwRu0FI6LyIa8Grzg59zdP9AnJOUee4130_assertion SIO_000772 16876867 NP869499.RAi6K6e_zf5ZFnbwRu0FI6LyIa8Grzg59zdP9AnJOUee4130_provenance.
- NP869499.RAi6K6e_zf5ZFnbwRu0FI6LyIa8Grzg59zdP9AnJOUee4130_assertion evidence source_evidence_literature NP869499.RAi6K6e_zf5ZFnbwRu0FI6LyIa8Grzg59zdP9AnJOUee4130_provenance.
- NP869499.RAi6K6e_zf5ZFnbwRu0FI6LyIa8Grzg59zdP9AnJOUee4130_assertion description "[A novel PITX2 mutation and a polymorphism in a 5-generation family with Axenfeld-Rieger anomaly and coexisting Fuchs' endothelial dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869499.RAi6K6e_zf5ZFnbwRu0FI6LyIa8Grzg59zdP9AnJOUee4130_provenance.