Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_provenance.
- NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_assertion wasGeneratedBy ECO_0000203 NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_provenance.
- NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_assertion wasDerivedFrom befree-20140225 NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_provenance.
- NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_assertion SIO_000772 19657220 NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_provenance.
- NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_assertion evidence source_evidence_literature NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_provenance.
- NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_assertion description "[The aim of this study was to determine for the first time the significance of PRSS1, SPINK1 mutations and genetic variants of AAT in a group of Spanish patients with CP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP393181.RAfz9KxdQrCe1GbuzuceZhL5LynCMVmWnWLb-s9r-uDIA130_provenance.