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- NP4837.RARZLbX-BSu1IFIZAsjl7n0_RSVT7B8ZXUxok2yVeCoRk130_assertion type Assertion NP4837.RARZLbX-BSu1IFIZAsjl7n0_RSVT7B8ZXUxok2yVeCoRk130_head.
- NP4837.RARZLbX-BSu1IFIZAsjl7n0_RSVT7B8ZXUxok2yVeCoRk130_assertion wasGeneratedBy ECO_0000218 NP4837.RARZLbX-BSu1IFIZAsjl7n0_RSVT7B8ZXUxok2yVeCoRk130_provenance.
- NP4837.RARZLbX-BSu1IFIZAsjl7n0_RSVT7B8ZXUxok2yVeCoRk130_assertion wasDerivedFrom uniprot-2016 NP4837.RARZLbX-BSu1IFIZAsjl7n0_RSVT7B8ZXUxok2yVeCoRk130_provenance.
- NP4837.RARZLbX-BSu1IFIZAsjl7n0_RSVT7B8ZXUxok2yVeCoRk130_assertion SIO_000772 17236141 NP4837.RARZLbX-BSu1IFIZAsjl7n0_RSVT7B8ZXUxok2yVeCoRk130_provenance.
- NP4837.RARZLbX-BSu1IFIZAsjl7n0_RSVT7B8ZXUxok2yVeCoRk130_assertion evidence source_evidence_curated NP4837.RARZLbX-BSu1IFIZAsjl7n0_RSVT7B8ZXUxok2yVeCoRk130_provenance.
- NP4837.RARZLbX-BSu1IFIZAsjl7n0_RSVT7B8ZXUxok2yVeCoRk130_assertion description "[Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4837.RARZLbX-BSu1IFIZAsjl7n0_RSVT7B8ZXUxok2yVeCoRk130_provenance.