Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_provenance.
- NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_assertion description "[This study describes the use of DHPLC for mutation analysis for BRCA1, BRCA2 and CHEK2 (1100delC) in 22 patients with a family history of breast and/or ovarian cancer and early onset breast cancer (<35 years of age).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_provenance.
- NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_assertion evidence source_evidence_literature NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_provenance.
- NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_assertion SIO_000772 14507240 NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_provenance.
- NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_assertion wasDerivedFrom befree-2016 NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_provenance.
- NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_assertion wasGeneratedBy ECO_0000203 NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_provenance.
- befree-2016 importedOn "2016-02-19" NP414389.RAAhcXwQlxJyLY8LwtjMkVFWvbjwUytPMSV8gy0Azb5W4130_provenance.