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- source_evidence_literature type ECO_0000212 NP404799.RA065empqnWKPWaMItIAoBEdPCxW_vvENokY_sB6oNBc4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404799.RA065empqnWKPWaMItIAoBEdPCxW_vvENokY_sB6oNBc4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404799.RA065empqnWKPWaMItIAoBEdPCxW_vvENokY_sB6oNBc4130_provenance.
- NP404799.RA065empqnWKPWaMItIAoBEdPCxW_vvENokY_sB6oNBc4130_assertion description "[FOXC2 represents the second known gene to result in hereditary lymphedema, and LD is only the second hereditary disorder known to be caused by a mutation in a forkhead-family gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404799.RA065empqnWKPWaMItIAoBEdPCxW_vvENokY_sB6oNBc4130_provenance.
- NP404799.RA065empqnWKPWaMItIAoBEdPCxW_vvENokY_sB6oNBc4130_assertion evidence source_evidence_literature NP404799.RA065empqnWKPWaMItIAoBEdPCxW_vvENokY_sB6oNBc4130_provenance.
- NP404799.RA065empqnWKPWaMItIAoBEdPCxW_vvENokY_sB6oNBc4130_assertion SIO_000772 11078474 NP404799.RA065empqnWKPWaMItIAoBEdPCxW_vvENokY_sB6oNBc4130_provenance.
- NP404799.RA065empqnWKPWaMItIAoBEdPCxW_vvENokY_sB6oNBc4130_assertion wasDerivedFrom befree-20150227 NP404799.RA065empqnWKPWaMItIAoBEdPCxW_vvENokY_sB6oNBc4130_provenance.
- NP404799.RA065empqnWKPWaMItIAoBEdPCxW_vvENokY_sB6oNBc4130_assertion wasGeneratedBy ECO_0000203 NP404799.RA065empqnWKPWaMItIAoBEdPCxW_vvENokY_sB6oNBc4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP404799.RA065empqnWKPWaMItIAoBEdPCxW_vvENokY_sB6oNBc4130_provenance.