Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_provenance.
- NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_assertion description "[Mutations in eight genes (ABCC8, KCNJ11, GLUD1, GCK, HADH, SLC16A1, HNF4A and HNF1A) are known to cause CHI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_provenance.
- NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_assertion evidence source_evidence_literature NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_provenance.
- NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_assertion SIO_000772 23345197 NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_provenance.
- NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_assertion wasDerivedFrom befree-20140225 NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_provenance.
- NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_assertion wasGeneratedBy ECO_0000203 NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP348531.RASZzFTlGiMfq6ErKk4QiqxlsBcnaTfqP39_uPqfvCM7U130_provenance.