Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_provenance.
- NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_assertion description "[In this study, we investigated the DNA sequences of BCKDHA, BCKDHB and DBT genes for mutations in a Chinese newborn with the classic form of MSUD and predicted the associated conformational changes using molecular modeling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_provenance.
- NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_assertion evidence source_evidence_literature NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_provenance.
- NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_assertion SIO_000772 22326532 NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_provenance.
- NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_assertion wasDerivedFrom befree-2016 NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_provenance.
- NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_assertion wasGeneratedBy ECO_0000203 NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_provenance.
- befree-2016 importedOn "2016-02-19" NP960203.RANe-_qBqBXfoTioSFP7bVDRe3vBudbfj0kTlVEyCpmvc130_provenance.