Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_provenance.
- NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_assertion description "[In summary, although heterozygous loss-of- function mutations in AKT2 can cause a syndrome of severe insulin resistance and lipodystrophy in humans, such mutations are uncommon causes of these syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_provenance.
- NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_assertion evidence source_evidence_literature NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_provenance.
- NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_assertion SIO_000772 17327441 NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_provenance.
- NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_assertion wasDerivedFrom befree-20140225 NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_provenance.
- NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_assertion wasGeneratedBy ECO_0000203 NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_provenance.
- befree-20140225 importedOn "2014-02-25" NP172515.RAwGOVZ5d9EWRdAcZSA323EOoymPSlO7pPM7rdtcGxHik130_provenance.