Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP802647.RAy6g6obkulE-NkWVCpw3umZot2cq6Xv7wVmv7Pw4DoUI130_provenance.
- 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.