Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_provenance.
- NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_assertion description "[In the course of positional cloning of the Congenital Dyserythropoietic Anemia type I (CDAI) [MIM 224120] gene on 15q15.1-15.3, we examined a family of French origin, in which the propositus suffered from asthenoteratozoospermia and nonsyndromic deafness in addition to CDAI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_provenance.
- NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_assertion evidence source_evidence_literature NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_provenance.
- NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_assertion SIO_000772 12825070 NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_provenance.
- NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_assertion wasDerivedFrom befree-20140225 NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_provenance.
- NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_assertion wasGeneratedBy ECO_0000203 NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP630263.RAqWqT9LQrATaXNAsdFK9kNOsO_8I3LtR01_wk0JB07pM130_provenance.