Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_provenance.
- NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_assertion wasGeneratedBy ECO_0000203 NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_provenance.
- NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_assertion wasDerivedFrom befree-20150227 NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_provenance.
- NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_assertion SIO_000772 9694901 NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_provenance.
- NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_assertion evidence source_evidence_literature NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_provenance.
- NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_assertion description "[The GM2 gangliosidoses are caused by mutations in the genes encoding the alpha- (Tay-Sachs) or beta- (Sandhoff) subunits of heterodimeric beta-hexosaminidase A (Hex A), or the GM2 activator protein (AB variant), a substrate-specific co-factor for Hex A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852073.RAeeXKllV1axyQ_5KrTs1aaWkfpH12tF8mYXH-OJdPKcA130_provenance.