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- source_evidence_literature type ECO_0000212 NP609918.RAE9VIeBMYJqmJw906Z0SjPDHth_iN9kuhCw3SJqfEUto130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609918.RAE9VIeBMYJqmJw906Z0SjPDHth_iN9kuhCw3SJqfEUto130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609918.RAE9VIeBMYJqmJw906Z0SjPDHth_iN9kuhCw3SJqfEUto130_provenance.
- NP609918.RAE9VIeBMYJqmJw906Z0SjPDHth_iN9kuhCw3SJqfEUto130_assertion description "[Autosomal recessive spastic paraplegias (ARHSPs) usually have clinically complex phenotypes but the SPG5, SPG24, and SPG28 loci are considered to be associated with pure forms of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609918.RAE9VIeBMYJqmJw906Z0SjPDHth_iN9kuhCw3SJqfEUto130_provenance.
- NP609918.RAE9VIeBMYJqmJw906Z0SjPDHth_iN9kuhCw3SJqfEUto130_assertion evidence source_evidence_literature NP609918.RAE9VIeBMYJqmJw906Z0SjPDHth_iN9kuhCw3SJqfEUto130_provenance.
- NP609918.RAE9VIeBMYJqmJw906Z0SjPDHth_iN9kuhCw3SJqfEUto130_assertion SIO_000772 17503452 NP609918.RAE9VIeBMYJqmJw906Z0SjPDHth_iN9kuhCw3SJqfEUto130_provenance.
- NP609918.RAE9VIeBMYJqmJw906Z0SjPDHth_iN9kuhCw3SJqfEUto130_assertion wasDerivedFrom befree-2016 NP609918.RAE9VIeBMYJqmJw906Z0SjPDHth_iN9kuhCw3SJqfEUto130_provenance.
- NP609918.RAE9VIeBMYJqmJw906Z0SjPDHth_iN9kuhCw3SJqfEUto130_assertion wasGeneratedBy ECO_0000203 NP609918.RAE9VIeBMYJqmJw906Z0SjPDHth_iN9kuhCw3SJqfEUto130_provenance.
- befree-2016 importedOn "2016-02-19" NP609918.RAE9VIeBMYJqmJw906Z0SjPDHth_iN9kuhCw3SJqfEUto130_provenance.