Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_provenance.
- NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_assertion description "[A variety of previously unreported mutations in the coding region of the CHST6 gene are associated with type I MCD in a cohort of patients in southern India.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_provenance.
- NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_assertion evidence source_evidence_curated NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_provenance.
- NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_assertion SIO_000772 14609920 NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_provenance.
- NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_assertion wasDerivedFrom uniprot-2016 NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_provenance.
- NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_assertion wasGeneratedBy ECO_0000218 NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3087.RAHdzEFnnOVzvFUojdToJCFz2_Vvxz47e_7F7diTx3Blo130_provenance.