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- source_evidence_literature type ECO_0000212 NP456993.RAqdUukS8-Rx3HS_FqGanrbuKafs5rgF1IKFLhz-Ie1Mk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP456993.RAqdUukS8-Rx3HS_FqGanrbuKafs5rgF1IKFLhz-Ie1Mk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP456993.RAqdUukS8-Rx3HS_FqGanrbuKafs5rgF1IKFLhz-Ie1Mk130_provenance.
- NP456993.RAqdUukS8-Rx3HS_FqGanrbuKafs5rgF1IKFLhz-Ie1Mk130_assertion description "[Infantile hereditary spastic paraparesis due to codominant mutations in the spastin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP456993.RAqdUukS8-Rx3HS_FqGanrbuKafs5rgF1IKFLhz-Ie1Mk130_provenance.
- NP456993.RAqdUukS8-Rx3HS_FqGanrbuKafs5rgF1IKFLhz-Ie1Mk130_assertion evidence source_evidence_literature NP456993.RAqdUukS8-Rx3HS_FqGanrbuKafs5rgF1IKFLhz-Ie1Mk130_provenance.
- NP456993.RAqdUukS8-Rx3HS_FqGanrbuKafs5rgF1IKFLhz-Ie1Mk130_assertion SIO_000772 15326248 NP456993.RAqdUukS8-Rx3HS_FqGanrbuKafs5rgF1IKFLhz-Ie1Mk130_provenance.
- NP456993.RAqdUukS8-Rx3HS_FqGanrbuKafs5rgF1IKFLhz-Ie1Mk130_assertion wasDerivedFrom befree-2016 NP456993.RAqdUukS8-Rx3HS_FqGanrbuKafs5rgF1IKFLhz-Ie1Mk130_provenance.
- NP456993.RAqdUukS8-Rx3HS_FqGanrbuKafs5rgF1IKFLhz-Ie1Mk130_assertion wasGeneratedBy ECO_0000203 NP456993.RAqdUukS8-Rx3HS_FqGanrbuKafs5rgF1IKFLhz-Ie1Mk130_provenance.
- befree-2016 importedOn "2016-02-19" NP456993.RAqdUukS8-Rx3HS_FqGanrbuKafs5rgF1IKFLhz-Ie1Mk130_provenance.