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- NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_assertion type Assertion NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_head.
- NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_assertion wasGeneratedBy ECO_0000203 NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance.
- NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_assertion wasDerivedFrom befree-20140225 NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance.
- NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_assertion SIO_000772 22152678 NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance.
- NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_assertion evidence source_evidence_literature NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance.
- NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_assertion description "[We used whole-exome sequencing of five unrelated individuals with lepto-SEMDJL to identify mutations in KIF22 as the cause of this skeletal condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597309.RA1uRE3segYkqksLtdjPFh5mnoQu9e1gg1jIAF0ri5KDc130_provenance.