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- NP622593.RAZ_c5mLtnc7R9oW5h1tzmBNMxRJHDrZ9OVDJvtjBfoc8130_assertion type Assertion NP622593.RAZ_c5mLtnc7R9oW5h1tzmBNMxRJHDrZ9OVDJvtjBfoc8130_head.
- NP622593.RAZ_c5mLtnc7R9oW5h1tzmBNMxRJHDrZ9OVDJvtjBfoc8130_assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP622593.RAZ_c5mLtnc7R9oW5h1tzmBNMxRJHDrZ9OVDJvtjBfoc8130_provenance.
- NP622593.RAZ_c5mLtnc7R9oW5h1tzmBNMxRJHDrZ9OVDJvtjBfoc8130_assertion evidence source_evidence_literature NP622593.RAZ_c5mLtnc7R9oW5h1tzmBNMxRJHDrZ9OVDJvtjBfoc8130_provenance.
- NP622593.RAZ_c5mLtnc7R9oW5h1tzmBNMxRJHDrZ9OVDJvtjBfoc8130_assertion SIO_000772 17665217 NP622593.RAZ_c5mLtnc7R9oW5h1tzmBNMxRJHDrZ9OVDJvtjBfoc8130_provenance.
- NP622593.RAZ_c5mLtnc7R9oW5h1tzmBNMxRJHDrZ9OVDJvtjBfoc8130_assertion wasDerivedFrom befree-2016 NP622593.RAZ_c5mLtnc7R9oW5h1tzmBNMxRJHDrZ9OVDJvtjBfoc8130_provenance.
- NP622593.RAZ_c5mLtnc7R9oW5h1tzmBNMxRJHDrZ9OVDJvtjBfoc8130_assertion wasGeneratedBy ECO_0000203 NP622593.RAZ_c5mLtnc7R9oW5h1tzmBNMxRJHDrZ9OVDJvtjBfoc8130_provenance.