Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_provenance.
- NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_assertion description "[PRSS1 mutations were identified mainly in CP patients (9.6% of CP vs 2.5% of ARP alleles, P = 0.094), whereas N34S SPINK1 mutation was present with comparable frequency in CP and ARP patients (7.7% vs 10.0%, P = 0.768).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_provenance.
- NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_assertion evidence source_evidence_literature NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_provenance.
- NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_assertion SIO_000772 16954950 NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_provenance.
- NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_assertion wasDerivedFrom befree-20150227 NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_provenance.
- NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_assertion wasGeneratedBy ECO_0000203 NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP649458.RA0hA84TlHocwV3NqBrImTbu8N6Z8l3R5thawuXssX8K4130_provenance.