Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_provenance.
- NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_assertion description "[Recently, reports of deletions and duplications flanked by BP1 and BP2 suggest an association with speech and motor delays, behavioral problems, seizures, and autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_provenance.
- NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_assertion evidence source_evidence_literature NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_provenance.
- NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_assertion SIO_000772 21359847 NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_provenance.
- NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_assertion wasDerivedFrom befree-20140225 NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_provenance.
- NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_assertion wasGeneratedBy ECO_0000203 NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP791523.RAc29VtNbIpDvmHiRPVeFGsJbCWyQWZwUhuFK94V54iKs130_provenance.