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- source_evidence_literature type ECO_0000212 NP1316503.RAD_jSjqTYd3K6PEv_m9OI5GtUBBSHhn3KzSf7mgdItGo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1316503.RAD_jSjqTYd3K6PEv_m9OI5GtUBBSHhn3KzSf7mgdItGo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1316503.RAD_jSjqTYd3K6PEv_m9OI5GtUBBSHhn3KzSf7mgdItGo130_provenance.
- NP1316503.RAD_jSjqTYd3K6PEv_m9OI5GtUBBSHhn3KzSf7mgdItGo130_assertion description "[Sequencing of the arylsulfatase A gene in a late infantile metachromatic leukodystrophy patient showed the presence of a 12-bp deletion in exon 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316503.RAD_jSjqTYd3K6PEv_m9OI5GtUBBSHhn3KzSf7mgdItGo130_provenance.
- NP1316503.RAD_jSjqTYd3K6PEv_m9OI5GtUBBSHhn3KzSf7mgdItGo130_assertion evidence source_evidence_literature NP1316503.RAD_jSjqTYd3K6PEv_m9OI5GtUBBSHhn3KzSf7mgdItGo130_provenance.
- NP1316503.RAD_jSjqTYd3K6PEv_m9OI5GtUBBSHhn3KzSf7mgdItGo130_assertion SIO_000772 7649558 NP1316503.RAD_jSjqTYd3K6PEv_m9OI5GtUBBSHhn3KzSf7mgdItGo130_provenance.
- NP1316503.RAD_jSjqTYd3K6PEv_m9OI5GtUBBSHhn3KzSf7mgdItGo130_assertion wasDerivedFrom befree-2016 NP1316503.RAD_jSjqTYd3K6PEv_m9OI5GtUBBSHhn3KzSf7mgdItGo130_provenance.
- NP1316503.RAD_jSjqTYd3K6PEv_m9OI5GtUBBSHhn3KzSf7mgdItGo130_assertion wasGeneratedBy ECO_0000203 NP1316503.RAD_jSjqTYd3K6PEv_m9OI5GtUBBSHhn3KzSf7mgdItGo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1316503.RAD_jSjqTYd3K6PEv_m9OI5GtUBBSHhn3KzSf7mgdItGo130_provenance.