Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_provenance.
- NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_assertion description "[Carrier testing was performed in 35 women belonging to 16 unrelated Spanish families with at least one subject affected by the Lesch-Nyhan syndrome (11 families, 14 patients) or the Kelley-Seegmiller syndrome (five families, six patients) by means of HPRT and adenine phosphoribosyltransferase activities in hair follicles and/or molecular studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_provenance.
- NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_assertion evidence source_evidence_literature NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_provenance.
- NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_assertion SIO_000772 9824441 NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_provenance.
- NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_assertion wasDerivedFrom befree-20140225 NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_provenance.
- NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_assertion wasGeneratedBy ECO_0000203 NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP773506.RAv4Op4OaSt74CqHf_zmxbc8lMs0RYyjeqSRwbBZvWh-k130_provenance.