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- NP1099013.RA1q_BUfcJfF-sCrLYyD-FKJIWZ_26zED0JvtegO5vhC8130_assertion type Assertion NP1099013.RA1q_BUfcJfF-sCrLYyD-FKJIWZ_26zED0JvtegO5vhC8130_head.
- NP1099013.RA1q_BUfcJfF-sCrLYyD-FKJIWZ_26zED0JvtegO5vhC8130_assertion description "[Analysis of an additional 54 skeletal ciliopathy exomes identified compound heterozygous mutations in WDR60 in a Spanish individual with Jeune syndrome of relatively mild presentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1099013.RA1q_BUfcJfF-sCrLYyD-FKJIWZ_26zED0JvtegO5vhC8130_provenance.
- NP1099013.RA1q_BUfcJfF-sCrLYyD-FKJIWZ_26zED0JvtegO5vhC8130_assertion evidence source_evidence_literature NP1099013.RA1q_BUfcJfF-sCrLYyD-FKJIWZ_26zED0JvtegO5vhC8130_provenance.
- NP1099013.RA1q_BUfcJfF-sCrLYyD-FKJIWZ_26zED0JvtegO5vhC8130_assertion SIO_000772 23910462 NP1099013.RA1q_BUfcJfF-sCrLYyD-FKJIWZ_26zED0JvtegO5vhC8130_provenance.
- NP1099013.RA1q_BUfcJfF-sCrLYyD-FKJIWZ_26zED0JvtegO5vhC8130_assertion wasDerivedFrom befree-2016 NP1099013.RA1q_BUfcJfF-sCrLYyD-FKJIWZ_26zED0JvtegO5vhC8130_provenance.
- NP1099013.RA1q_BUfcJfF-sCrLYyD-FKJIWZ_26zED0JvtegO5vhC8130_assertion wasGeneratedBy ECO_0000203 NP1099013.RA1q_BUfcJfF-sCrLYyD-FKJIWZ_26zED0JvtegO5vhC8130_provenance.