Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_provenance.
- NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_assertion description "[When the mutation is located on chromosome 16 (PKD1), extra-renal manifestations such as the rupture of intracranial aneurysms are well known.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_provenance.
- NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_assertion evidence source_evidence_literature NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_provenance.
- NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_assertion SIO_000772 8749697 NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_provenance.
- NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_assertion wasDerivedFrom befree-20140225 NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_provenance.
- NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_assertion wasGeneratedBy ECO_0000203 NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP239925.RAei4OoqbfltOIaVUup-g_J0_skQlgwF-wcTBOgbuzTvM130_provenance.