Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_provenance.
- NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_assertion description "[Mutations in SUR1 are the cause of about 15% of Kir6.2 negative permanent ND in Poland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_provenance.
- NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_assertion evidence source_evidence_literature NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_provenance.
- NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_assertion SIO_000772 19021632 NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_provenance.
- NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_assertion wasDerivedFrom befree-20140225 NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_provenance.
- NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_assertion wasGeneratedBy ECO_0000203 NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP273390.RAZ4qlF2z-W-cf25VRaLc2Ez3qniFe9xQMPR-uO5PQOuQ130_provenance.