Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_provenance.
- NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_assertion description "[Mutations in the Norrie Disease gene, Norrie Disease Pseudoglioma (NDP) lead to a phenotypically heterogeneous group of retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_provenance.
- NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_assertion evidence source_evidence_literature NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_provenance.
- NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_assertion SIO_000772 19373682 NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_provenance.
- NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_assertion wasDerivedFrom befree-20150227 NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_provenance.
- NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_assertion wasGeneratedBy ECO_0000203 NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP585877.RAHb-0LdBqK_-CcccP4F-PLlAMbqCn76WG48B6ZMz77qo130_provenance.