Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_provenance.
- NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_assertion wasGeneratedBy ECO_0000203 NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_provenance.
- NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_assertion wasDerivedFrom befree-20150227 NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_provenance.
- NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_assertion SIO_000772 18682420 NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_provenance.
- NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_assertion evidence source_evidence_literature NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_provenance.
- NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_assertion description "[In this review we will focus on the hereditary breast carcinomas caused by mutations in BRCA1, BRCA2, Fanconi anaemia (FANC) genes, CHK2 and ATM tumour suppressor genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862701.RAmBWu6ukvhUcXQAPv9urdvqI-J4zVHru-M_wJjC37g9I130_provenance.