Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_provenance.
- NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_assertion description "[in the investigated Finnish pedigree with hereditary pancreatitis, the PRSS1 mutation R122H is linked with chronic disease; although the SPINK1 mutation (N34S) was also observed in two individuals, it was not linked with the disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_provenance.
- NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_assertion evidence source_evidence_literature NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_provenance.
- NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_assertion SIO_000772 17613931 NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_provenance.
- NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_assertion wasDerivedFrom lhgdn-20090331 NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_provenance.
- NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_assertion wasGeneratedBy ECO_0000203 NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP226913.RAeuFWN9jf_fwGPiBcS9L4YMthl1TbhVonR1nHB5oXFfA130_provenance.