Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_provenance.
- NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_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." NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_provenance.
- NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_assertion evidence source_evidence_curated NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_provenance.
- NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_assertion SIO_000772 12142464 NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_provenance.
- NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_assertion wasDerivedFrom uniprot-2016 NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_provenance.
- NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_assertion wasGeneratedBy ECO_0000218 NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP2165.RAEgcFs423RBYqcIKJq-i_iMiIdxL25gbAJmscogZYiyA130_provenance.