Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_provenance.
- NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_assertion wasGeneratedBy ECO_0000203 NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_provenance.
- NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_assertion wasDerivedFrom befree-20150227 NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_provenance.
- NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_assertion SIO_000772 22894767 NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_provenance.
- NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_assertion evidence source_evidence_literature NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_provenance.
- NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_assertion description "[A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_provenance.