Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_provenance.
- NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_assertion description "[The recently described mutations in NPHP1, encoding a protein containing an SH3 domain, in a subset of patients with JS plus nephronophthisis, suggest a shared pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_provenance.
- NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_assertion evidence source_evidence_literature NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_provenance.
- NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_assertion SIO_000772 15467982 NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_provenance.
- NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_assertion wasDerivedFrom befree-2016 NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_provenance.
- NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_assertion wasGeneratedBy ECO_0000203 NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_provenance.
- befree-2016 importedOn "2016-02-19" NP463306.RAoM93bfpWnDeCnAkdDSjB7rMapw8N28R0tKKce7NtyZg130_provenance.