Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_provenance.
- NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_assertion description "[Finally, twelve studies were included for FVL and nine studies were included for G20210A prothrombin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_provenance.
- NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_assertion evidence source_evidence_literature NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_provenance.
- NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_assertion SIO_000772 24755609 NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_provenance.
- NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_assertion wasDerivedFrom befree-2016 NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_provenance.
- NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_assertion wasGeneratedBy ECO_0000203 NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_provenance.
- befree-2016 importedOn "2016-02-19" NP1175762.RAfNq6LGaB9nU6NNKKgfIV4eNT3e2aycaOnKlcfOgPQ1M130_provenance.