Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP649382.RAREcLD7uSw7NTrsnOQIejtrbAHdyHMbQEx4Vl4Nzgu-E130_assertion> ?p ?o ?g. }
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- NP649382.RAREcLD7uSw7NTrsnOQIejtrbAHdyHMbQEx4Vl4Nzgu-E130_assertion type Assertion NP649382.RAREcLD7uSw7NTrsnOQIejtrbAHdyHMbQEx4Vl4Nzgu-E130_head.
- NP649382.RAREcLD7uSw7NTrsnOQIejtrbAHdyHMbQEx4Vl4Nzgu-E130_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." NP649382.RAREcLD7uSw7NTrsnOQIejtrbAHdyHMbQEx4Vl4Nzgu-E130_provenance.
- NP649382.RAREcLD7uSw7NTrsnOQIejtrbAHdyHMbQEx4Vl4Nzgu-E130_assertion evidence source_evidence_literature NP649382.RAREcLD7uSw7NTrsnOQIejtrbAHdyHMbQEx4Vl4Nzgu-E130_provenance.
- NP649382.RAREcLD7uSw7NTrsnOQIejtrbAHdyHMbQEx4Vl4Nzgu-E130_assertion SIO_000772 17613931 NP649382.RAREcLD7uSw7NTrsnOQIejtrbAHdyHMbQEx4Vl4Nzgu-E130_provenance.
- NP649382.RAREcLD7uSw7NTrsnOQIejtrbAHdyHMbQEx4Vl4Nzgu-E130_assertion wasDerivedFrom befree-20150227 NP649382.RAREcLD7uSw7NTrsnOQIejtrbAHdyHMbQEx4Vl4Nzgu-E130_provenance.
- NP649382.RAREcLD7uSw7NTrsnOQIejtrbAHdyHMbQEx4Vl4Nzgu-E130_assertion wasGeneratedBy ECO_0000203 NP649382.RAREcLD7uSw7NTrsnOQIejtrbAHdyHMbQEx4Vl4Nzgu-E130_provenance.