Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance.
- NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_assertion description "[In the remaining 5 individuals with PCD who underwent exome sequencing, we identified mutations in two genes (DNAI2, DNAH5) known to cause PCD, including an Ashkenazi Jewish founder mutation in DNAI2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance.
- NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_assertion evidence source_evidence_literature NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance.
- NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_assertion SIO_000772 23261302 NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance.
- NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_assertion wasDerivedFrom befree-2016 NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance.
- NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_assertion wasGeneratedBy ECO_0000203 NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance.
- befree-2016 importedOn "2016-02-19" NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance.