Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_provenance.
- NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_assertion description "[Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_provenance.
- NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_assertion evidence source_evidence_curated NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_provenance.
- NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_assertion SIO_000772 10617473 NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_provenance.
- NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_assertion wasDerivedFrom uniprot-2016 NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_provenance.
- NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_assertion wasGeneratedBy ECO_0000218 NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP567.RATcfem0W3MFdpoZkYj6f68MbKxubhTZZACYTUl5IvvvI130_provenance.