Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_assertion> ?p ?o ?g. }
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- NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_assertion type Assertion NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_head.
- NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_assertion wasGeneratedBy ECO_0000203 NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_provenance.
- NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_assertion wasDerivedFrom befree-20150227 NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_provenance.
- NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_assertion SIO_000772 23297359 NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_provenance.
- NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_assertion evidence source_evidence_literature NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_provenance.
- NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_assertion description "[We subsequently sequenced CTSF in 22 unrelated individuals with suspected recessive Kufs disease, and identified an additional patient with compound heterozygous mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_provenance.