Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_provenance.
- NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_assertion description "[Congenital risk factors include deficiencies or defects in natural anticoagulants, such as antithrombin, protein C and protein S, and genetic polymorphisms such as prothrombin G20210A and the cleavage-resistant factor mutation, factor V Leiden, which leads to a condition known as activated protein C resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_provenance.
- NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_assertion evidence source_evidence_literature NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_provenance.
- NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_assertion SIO_000772 15706470 NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_provenance.
- NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_assertion wasDerivedFrom befree-20150227 NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_provenance.
- NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_assertion wasGeneratedBy ECO_0000203 NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP389789.RAhK3THo1U2BfIfIxj9FpHGIGBIdntd1yGNxdUeJqU_wU130_provenance.