Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_provenance.
- NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_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." NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_provenance.
- NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_assertion evidence source_evidence_literature NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_provenance.
- NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_assertion SIO_000772 18987270 NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_provenance.
- NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_assertion wasDerivedFrom befree-20150227 NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_provenance.
- NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_assertion wasGeneratedBy ECO_0000203 NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP534016.RAV3z7KkVnnXBMe8YZW9vp7VmRBzOk0IKK__SdOsUbkoI130_provenance.