Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_provenance.
- NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_assertion description "[A test set comprising 9 BRCA1 germline mutants and 14 high-grade serous carcinoma controls lacking BRCA1 and BRCA2 germline mutation was used to validate the algorithms, with specific emphasis on the ability to detect cases with BRCA1 germline mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_provenance.
- NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_assertion evidence source_evidence_literature NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_provenance.
- NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_assertion SIO_000772 22193042 NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_provenance.
- NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_assertion wasDerivedFrom befree-20140225 NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_provenance.
- NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_assertion wasGeneratedBy ECO_0000203 NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP828329.RAiBc9_KaY8J0Oa0SnHNDtYQkxZgcrdWS7_9cp0Ruzt-s130_provenance.