Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_provenance.
- NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_assertion description "[Two novel mutations in the arylsulfatase A (ASA) gene from a Japanese patient with the late-infantile form of metachromatic leukodystrophy (MLD) were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_provenance.
- NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_assertion evidence source_evidence_literature NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_provenance.
- NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_assertion SIO_000772 8891236 NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_provenance.
- NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_assertion wasDerivedFrom befree-2016 NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_provenance.
- NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_assertion wasGeneratedBy ECO_0000203 NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1361169.RAjWfHCXwKCvs22Z4qDu3zfUKrEAP3MuaDf4LEDtkD7tQ130_provenance.