Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_provenance.
- NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_assertion description "[MYH9-related disease ( MYH9-RD) is an autosomal dominant thrombocytopenia with giant platelets variably associated with young-adult onset of progressive sensorineural hearing loss, presenile cataract, and renal damage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_provenance.
- NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_assertion evidence source_evidence_literature NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_provenance.
- NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_assertion SIO_000772 20174760 NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_provenance.
- NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_assertion wasDerivedFrom befree-2016 NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_provenance.
- NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_assertion wasGeneratedBy ECO_0000203 NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP795163.RA0poFwC1rNAe9Xzp6UY1qDyeEcL7sg8niPMuUN6BfqPQ130_provenance.