Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_provenance.
- NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_assertion description "[In the investigated Finnish pedigree with HP, the PRSS1 mutation R122H is linked with chronic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_provenance.
- NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_assertion evidence source_evidence_literature NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_provenance.
- NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_assertion SIO_000772 17613931 NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_provenance.
- NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_assertion wasDerivedFrom befree-20140225 NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_provenance.
- NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_assertion wasGeneratedBy ECO_0000203 NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_provenance.