Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_provenance.
- NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_assertion description "[Specific mutations in the cationic trypsinogen gene ( PRSS1) are disease-causing in patients with hereditary pancreatitis, but the genetic background still remains mysterious in about 40% of patients with the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_provenance.
- NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_assertion evidence source_evidence_literature NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_provenance.
- NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_assertion SIO_000772 15338373 NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_provenance.
- NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_assertion wasDerivedFrom befree-2016 NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_provenance.
- NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_assertion wasGeneratedBy ECO_0000203 NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_provenance.
- befree-2016 importedOn "2016-02-19" NP458034.RAo5TTfcK88hGHP0JlCSUxhuZn4KQGCbqeJMaxvHsXPVg130_provenance.