Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_provenance.
- NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_assertion description "[The group of disorders manifesting as hereditary elliptocytosis/pyropoikilocytosis (HE/HPP) represent a unique group of experiments of nature that result from molecular defects of alpha spectrin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_provenance.
- NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_assertion evidence source_evidence_literature NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_provenance.
- NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_assertion SIO_000772 3311220 NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_provenance.
- NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_assertion wasDerivedFrom befree-20140225 NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_provenance.
- NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_assertion wasGeneratedBy ECO_0000203 NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP488582.RAx3ihbb_IoV4FBbZ1fRoZaIs7G-9zTfk5_fjldgXsECw130_provenance.