Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_provenance.
- NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_assertion description "[Mutations in human PEX12 result in Zellweger syndrome, a lethal neurological disorder, and implicate the zinc ring domain in PEX12 function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_provenance.
- NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_assertion evidence source_evidence_literature NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_provenance.
- NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_assertion SIO_000772 10562279 NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_provenance.
- NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_assertion wasDerivedFrom befree-20150227 NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_provenance.
- NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_assertion wasGeneratedBy ECO_0000203 NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP616339.RALgWuU73WEuFA1XVP5Uds5hAR5x5IYqC9UcvdQPdmB8w130_provenance.