Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_assertion> ?p ?o ?g. }
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- NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_assertion type Assertion NP333992.RAsnJe68NwUq5OkNsxDlcKeFof4jcCkuMjNvpKaa8R_jY130_head.
- 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.