Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_provenance.
- NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_assertion description "[Unexpectedly, we found that deleting exons 2-4 of Dyx1c1 in mice caused a phenotype resembling primary ciliary dyskinesia (PCD), a disorder characterized by chronic airway disease, laterality defects and male infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_provenance.
- NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_assertion evidence source_evidence_literature NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_provenance.
- NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_assertion SIO_000772 23872636 NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_provenance.
- NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_assertion wasDerivedFrom befree-20150227 NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_provenance.
- NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_assertion wasGeneratedBy ECO_0000203 NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977254.RAMEEaHzyyewtp3zegjUKeg6wMQdJvpWAw3r2vKa-2RT0130_provenance.