Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.
- NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_assertion description "[Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.
- NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_assertion evidence source_evidence_literature NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.
- NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_assertion SIO_000772 24767429 NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.
- NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_assertion wasDerivedFrom befree-20150227 NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.
- NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_assertion wasGeneratedBy ECO_0000203 NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936904.RAT0mYJBD-l2XTAYVl9FOD0X0v-ekZkGo2diS0Okh4n_c130_provenance.