Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_provenance.
- NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_assertion description "[Monogenic forms of disease explain 6% of children with extreme obesity, having hyperphagia associated with defects in the leptin-melanocortin pathway, as a central feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_provenance.
- NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_assertion evidence source_evidence_literature NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_provenance.
- NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_assertion SIO_000772 18987270 NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_provenance.
- NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_assertion wasDerivedFrom befree-2016 NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_provenance.
- NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_assertion wasGeneratedBy ECO_0000203 NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_provenance.
- befree-2016 importedOn "2016-02-19" NP701843.RAWJXISDtFTCsBX6duaucWDIlUULfMMQ7ka384iFMbMdo130_provenance.