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- source_evidence_literature type ECO_0000212 NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP947446.RAdPzY6_evWsn9NQqoNsh6d9x8dueJrMFcvjq31Rh7xPw130_provenance.