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- NP821033.RAmsVyv3slEzCVJjFwa-rkP6r7devS8cXwCCeLjDjIVTk130_assertion type Assertion NP821033.RAmsVyv3slEzCVJjFwa-rkP6r7devS8cXwCCeLjDjIVTk130_head.
- NP821033.RAmsVyv3slEzCVJjFwa-rkP6r7devS8cXwCCeLjDjIVTk130_assertion wasGeneratedBy ECO_0000203 NP821033.RAmsVyv3slEzCVJjFwa-rkP6r7devS8cXwCCeLjDjIVTk130_provenance.
- NP821033.RAmsVyv3slEzCVJjFwa-rkP6r7devS8cXwCCeLjDjIVTk130_assertion wasDerivedFrom befree-20140225 NP821033.RAmsVyv3slEzCVJjFwa-rkP6r7devS8cXwCCeLjDjIVTk130_provenance.
- NP821033.RAmsVyv3slEzCVJjFwa-rkP6r7devS8cXwCCeLjDjIVTk130_assertion SIO_000772 19860667 NP821033.RAmsVyv3slEzCVJjFwa-rkP6r7devS8cXwCCeLjDjIVTk130_provenance.
- NP821033.RAmsVyv3slEzCVJjFwa-rkP6r7devS8cXwCCeLjDjIVTk130_assertion evidence source_evidence_literature NP821033.RAmsVyv3slEzCVJjFwa-rkP6r7devS8cXwCCeLjDjIVTk130_provenance.
- NP821033.RAmsVyv3slEzCVJjFwa-rkP6r7devS8cXwCCeLjDjIVTk130_assertion description "[Non-syndromic, hereditary human cataract development is linked to point mutations in the CRYAA and CRYAB genes which encode alphaA and alphaB-crystallin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP821033.RAmsVyv3slEzCVJjFwa-rkP6r7devS8cXwCCeLjDjIVTk130_provenance.