Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_assertion> ?p ?o ?g. }
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- NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_assertion type Assertion NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_head.
- NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_assertion description "[Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_provenance.
- NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_assertion evidence source_evidence_literature NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_provenance.
- NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_assertion SIO_000772 22178368 NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_provenance.
- NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_assertion wasDerivedFrom befree-2016 NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_provenance.
- NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_assertion wasGeneratedBy ECO_0000203 NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_provenance.