Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance.
- NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_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." NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance.
- NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_assertion evidence source_evidence_literature NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance.
- NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_assertion SIO_000772 17327441 NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance.
- NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_assertion wasDerivedFrom befree-20150227 NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance.
- NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_assertion wasGeneratedBy ECO_0000203 NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP232977.RAygcanbs5iKuibI0CFYlgE6I2tqudaBOJg-xLJ0BQzO8130_provenance.