Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_provenance.
- NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_assertion description "[The influence of rare genetic variation in SLC30A8 on diabetes incidence and ?-cell function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_provenance.
- NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_assertion evidence source_evidence_literature NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_provenance.
- NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_assertion SIO_000772 24471563 NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_provenance.
- NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_assertion wasDerivedFrom befree-20150227 NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_provenance.
- NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_assertion wasGeneratedBy ECO_0000203 NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977956.RAi1_WOEsHrBy37iN6DeFz_GSrNNtTZABNSLmpsaUodVY130_provenance.