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- source_evidence_literature type ECO_0000212 NP1390057.RAaH8MFlD7mBHnWW1fzZpfhIv6n3umihDatVAfaPk2ghg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1390057.RAaH8MFlD7mBHnWW1fzZpfhIv6n3umihDatVAfaPk2ghg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1390057.RAaH8MFlD7mBHnWW1fzZpfhIv6n3umihDatVAfaPk2ghg130_provenance.
- NP1390057.RAaH8MFlD7mBHnWW1fzZpfhIv6n3umihDatVAfaPk2ghg130_assertion description "[Eluate showed a band with a mol wt of 14,000 and the N-terminal 14 amino acid residues of 14-kDa protein were identical with that of cystatin C. This molecular weight is not identical to that of the truncated form of cystatin C deposited in hereditary cerebral hemorrhage with amyloidosis in Iceland (HCHWA-I), but that of normal cystatin C. DNA sequence analysis of five patients showed no point mutations in the cystatin C gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1390057.RAaH8MFlD7mBHnWW1fzZpfhIv6n3umihDatVAfaPk2ghg130_provenance.
- NP1390057.RAaH8MFlD7mBHnWW1fzZpfhIv6n3umihDatVAfaPk2ghg130_assertion evidence source_evidence_literature NP1390057.RAaH8MFlD7mBHnWW1fzZpfhIv6n3umihDatVAfaPk2ghg130_provenance.
- NP1390057.RAaH8MFlD7mBHnWW1fzZpfhIv6n3umihDatVAfaPk2ghg130_assertion SIO_000772 9493177 NP1390057.RAaH8MFlD7mBHnWW1fzZpfhIv6n3umihDatVAfaPk2ghg130_provenance.
- NP1390057.RAaH8MFlD7mBHnWW1fzZpfhIv6n3umihDatVAfaPk2ghg130_assertion wasDerivedFrom befree-2016 NP1390057.RAaH8MFlD7mBHnWW1fzZpfhIv6n3umihDatVAfaPk2ghg130_provenance.
- NP1390057.RAaH8MFlD7mBHnWW1fzZpfhIv6n3umihDatVAfaPk2ghg130_assertion wasGeneratedBy ECO_0000203 NP1390057.RAaH8MFlD7mBHnWW1fzZpfhIv6n3umihDatVAfaPk2ghg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1390057.RAaH8MFlD7mBHnWW1fzZpfhIv6n3umihDatVAfaPk2ghg130_provenance.