Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_provenance.
- befree-2016 importedOn "2016-02-19" NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_provenance.
- NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_assertion wasGeneratedBy ECO_0000203 NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_provenance.
- NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_assertion wasDerivedFrom befree-2016 NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_provenance.
- NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_assertion SIO_000772 20507343 NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_provenance.
- NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_assertion evidence source_evidence_literature NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_provenance.
- NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_assertion description "[C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815220.RAiJMx3LZCIXWmU5jZrZJ_n-WFBKDPuGjNOsBchMtpHaE130_provenance.