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- NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_assertion type Assertion NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_head.
- NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_assertion wasGeneratedBy ECO_0000203 NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance.
- NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_assertion wasDerivedFrom befree-2016 NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance.
- NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_assertion SIO_000772 22152678 NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance.
- NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_assertion evidence source_evidence_literature NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance.
- NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_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." NP944913.RA5j9ASf6ALCwLRoPODyhwfIi6pG7mEhEiFu6pxVFI_IY130_provenance.