Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_provenance.
- NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_assertion description "[There may be more common mutations in other genes (such as ATM, HRAS1) that confer a moderate risk of breast cancer, and may account for 5 to 15 per cent of cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_provenance.
- NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_assertion evidence source_evidence_literature NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_provenance.
- NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_assertion SIO_000772 8987214 NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_provenance.
- NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_assertion wasDerivedFrom befree-2016 NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_provenance.
- NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_assertion wasGeneratedBy ECO_0000203 NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1365257.RAJ029oSpL4Jhw5opv3O05AOR9p_ELiHj0R5VPMZ8URvE130_provenance.