Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_provenance.
- NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_assertion description "[Charcot-Marie-Tooth disease type 4J (OMIM 611228) is a recessive, potentially severe form of the disease caused by mutations of the lipid phosphatase FIG4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_provenance.
- NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_assertion evidence source_evidence_literature NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_provenance.
- NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_assertion SIO_000772 21705420 NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_provenance.
- NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_assertion wasDerivedFrom befree-20140225 NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_provenance.
- NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_assertion wasGeneratedBy ECO_0000203 NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP519625.RA2vczDftuW2zkh0t48e33a4A-y0S_uhollXasFvQp32c130_provenance.