Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_provenance.
- NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_assertion description "[The FLCN mutation detection rate by bidirectional DNA sequencing in the National Cancer Institute BHDS cohort was 88%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_provenance.
- NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_assertion evidence source_evidence_literature NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_provenance.
- NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_assertion SIO_000772 21412933 NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_provenance.
- NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_assertion wasDerivedFrom befree-20150227 NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_provenance.
- NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_assertion wasGeneratedBy ECO_0000203 NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP979525.RAvhb9OnowqvIHfesQ0nLJzyazElTa42DSkt43Xdmj_xM130_provenance.