Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance.
- NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_assertion description "[This AIR pattern suggested a K(ATP) channel defect because it resembled that seen in children with recessive hyperinsulinism due to two common SUR1 mutations, g3992-9a and delPhe1388.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance.
- NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_assertion evidence source_evidence_literature NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance.
- NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_assertion SIO_000772 12941782 NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance.
- NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_assertion wasDerivedFrom befree-20140225 NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance.
- NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_assertion wasGeneratedBy ECO_0000203 NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP380764.RA3nPkrzi11ZvIht59X4azpbx-guz6sGctTYyKhYHkd8c130_provenance.