Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_provenance.
- NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_assertion description "[Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_provenance.
- NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_assertion evidence source_evidence_literature NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_provenance.
- NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_assertion SIO_000772 12142464 NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_provenance.
- NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_assertion wasDerivedFrom befree-20150227 NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_provenance.
- NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_assertion wasGeneratedBy ECO_0000203 NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP696590.RAAc5LqQruO2NAtibSYJqECW8Kv1jplNKgQ_WAbEpDTHg130_provenance.