Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_provenance.
- NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_assertion description "[All six IFT-A components and their motor protein, DYNC2H1, have been linked to human skeletal ciliopathies, including asphyxiating thoracic dystrophy (ATD; also known as Jeune syndrome), Sensenbrenner syndrome, and Mainzer-Saldino syndrome (MZSDS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_provenance.
- NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_assertion evidence source_evidence_literature NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_provenance.
- NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_assertion SIO_000772 24140113 NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_provenance.
- NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_assertion wasDerivedFrom befree-20140225 NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_provenance.
- NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_assertion wasGeneratedBy ECO_0000203 NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP534844.RA-dN_gLQk737WB6SnXCHiyoro48C6p_Kx1fGN0h9RmiY130_provenance.