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- source_evidence_literature type ECO_0000212 NP583631.RADkL6Jeje2IeODchMcGjtI7AlamkeOP7jTY64lg0P75E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583631.RADkL6Jeje2IeODchMcGjtI7AlamkeOP7jTY64lg0P75E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583631.RADkL6Jeje2IeODchMcGjtI7AlamkeOP7jTY64lg0P75E130_provenance.
- NP583631.RADkL6Jeje2IeODchMcGjtI7AlamkeOP7jTY64lg0P75E130_assertion description "[MYH9-associated disorders (May-Hegglin anomaly, Epstein and Fechtner syndrome, and others) are inherited in an autosomal dominant manner and characterized by defects in different organs (including eyes, ears, kidneys and thrombocytes).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583631.RADkL6Jeje2IeODchMcGjtI7AlamkeOP7jTY64lg0P75E130_provenance.
- NP583631.RADkL6Jeje2IeODchMcGjtI7AlamkeOP7jTY64lg0P75E130_assertion evidence source_evidence_literature NP583631.RADkL6Jeje2IeODchMcGjtI7AlamkeOP7jTY64lg0P75E130_provenance.
- NP583631.RADkL6Jeje2IeODchMcGjtI7AlamkeOP7jTY64lg0P75E130_assertion SIO_000772 23144074 NP583631.RADkL6Jeje2IeODchMcGjtI7AlamkeOP7jTY64lg0P75E130_provenance.
- NP583631.RADkL6Jeje2IeODchMcGjtI7AlamkeOP7jTY64lg0P75E130_assertion wasDerivedFrom befree-20150227 NP583631.RADkL6Jeje2IeODchMcGjtI7AlamkeOP7jTY64lg0P75E130_provenance.
- NP583631.RADkL6Jeje2IeODchMcGjtI7AlamkeOP7jTY64lg0P75E130_assertion wasGeneratedBy ECO_0000203 NP583631.RADkL6Jeje2IeODchMcGjtI7AlamkeOP7jTY64lg0P75E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583631.RADkL6Jeje2IeODchMcGjtI7AlamkeOP7jTY64lg0P75E130_provenance.