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- source_evidence_literature type ECO_0000212 NP406840.RAwF9-pS65Tyhk9VgF6A32ww50CdAELSdRDNa5GSmXFnQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406840.RAwF9-pS65Tyhk9VgF6A32ww50CdAELSdRDNa5GSmXFnQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406840.RAwF9-pS65Tyhk9VgF6A32ww50CdAELSdRDNa5GSmXFnQ130_provenance.
- NP406840.RAwF9-pS65Tyhk9VgF6A32ww50CdAELSdRDNa5GSmXFnQ130_assertion description "[These results indicate that hyperinsulinism in this family is caused by a SUR1 mutation that is expressed dominantly rather than recessively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406840.RAwF9-pS65Tyhk9VgF6A32ww50CdAELSdRDNa5GSmXFnQ130_provenance.
- NP406840.RAwF9-pS65Tyhk9VgF6A32ww50CdAELSdRDNa5GSmXFnQ130_assertion evidence source_evidence_literature NP406840.RAwF9-pS65Tyhk9VgF6A32ww50CdAELSdRDNa5GSmXFnQ130_provenance.
- NP406840.RAwF9-pS65Tyhk9VgF6A32ww50CdAELSdRDNa5GSmXFnQ130_assertion SIO_000772 12941782 NP406840.RAwF9-pS65Tyhk9VgF6A32ww50CdAELSdRDNa5GSmXFnQ130_provenance.
- NP406840.RAwF9-pS65Tyhk9VgF6A32ww50CdAELSdRDNa5GSmXFnQ130_assertion wasDerivedFrom befree-2016 NP406840.RAwF9-pS65Tyhk9VgF6A32ww50CdAELSdRDNa5GSmXFnQ130_provenance.
- NP406840.RAwF9-pS65Tyhk9VgF6A32ww50CdAELSdRDNa5GSmXFnQ130_assertion wasGeneratedBy ECO_0000203 NP406840.RAwF9-pS65Tyhk9VgF6A32ww50CdAELSdRDNa5GSmXFnQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP406840.RAwF9-pS65Tyhk9VgF6A32ww50CdAELSdRDNa5GSmXFnQ130_provenance.