Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_provenance.
- NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_assertion description "[This is the first study from South India, on BRCA1, BRCA2 & CHEK2 (1100 del C) mutations in patients with a family history of breast and/or ovarian cancer and early onset breast/ovarian cancer, using the sensitive DHPLC approach.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_provenance.
- NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_assertion evidence source_evidence_literature NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_provenance.
- NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_assertion SIO_000772 14507240 NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_provenance.
- NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_assertion wasDerivedFrom befree-20150227 NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_provenance.
- NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_assertion wasGeneratedBy ECO_0000203 NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP863008.RAb1ZjGi_RLtUSq3FIWhbEPxuG5AqZJSAb8IpDeUmjrvU130_provenance.