Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_provenance.
- NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_assertion description "[Novel presentations of congenital hyperinsulinism due to mutations in the MODY genes: HNF1A and HNF4A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_provenance.
- NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_assertion evidence source_evidence_literature NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_provenance.
- NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_assertion SIO_000772 22802087 NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_provenance.
- NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_assertion wasDerivedFrom befree-20140225 NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_provenance.
- NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_assertion wasGeneratedBy ECO_0000203 NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP260515.RApxEGxyp4tMGvHcK_ydVwuijgz3evfmv-Dyqw4AGrynE130_provenance.