Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_provenance.
- NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_assertion description "[WDR35 is homologous to TULP4 (from the Tubby superfamily) and has previously been characterized as an intraflagellar transport component, confirming that Sensenbrenner syndrome is a ciliary disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_provenance.
- NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_assertion evidence source_evidence_literature NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_provenance.
- NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_assertion SIO_000772 20817137 NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_provenance.
- NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_assertion wasDerivedFrom befree-2016 NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_provenance.
- NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_assertion wasGeneratedBy ECO_0000203 NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_provenance.
- befree-2016 importedOn "2016-02-19" NP837146.RAmq6YKIkTBR8M3y00T7Tk88ea1g7_1m_ZZ9TeqZPEEeY130_provenance.