Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_provenance.
- befree-2016 importedOn "2016-02-19" NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_provenance.
- NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_assertion wasGeneratedBy ECO_0000203 NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_provenance.
- NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_assertion wasDerivedFrom befree-2016 NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_provenance.
- NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_assertion SIO_000772 12868035 NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_provenance.
- NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_assertion evidence source_evidence_literature NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_provenance.
- NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_assertion description "[We screened the OA1 gene for mutations in three unrelated Canadian and French families and in two isolated patients with OA1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP402277.RAIEzmyLo0J-Iv1Ned7wsaeETrO8DOpm2VsfkiQjTfebY130_provenance.