Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_provenance.
- NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_assertion description "[The diagnosis of CNL will no longer be one only of exclusion, and revision of the current WHO diagnostic criteria is expected to include the molecular criterion of CSF3R mutation positivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_provenance.
- NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_assertion evidence source_evidence_literature NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_provenance.
- NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_assertion SIO_000772 24335708 NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_provenance.
- NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_assertion wasDerivedFrom befree-20150227 NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_provenance.
- NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_assertion wasGeneratedBy ECO_0000203 NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP332141.RAq9nqDIOyAjIjTAM9Bt8EUfXG5xdYiCJ4SFNfnHrW3VM130_provenance.