Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_provenance.
- NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_assertion description "[CACNA1H mutations in autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_provenance.
- NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_assertion evidence source_evidence_literature NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_provenance.
- NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_assertion SIO_000772 16754686 NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_provenance.
- NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_assertion wasDerivedFrom befree-2016 NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_provenance.
- NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_assertion wasGeneratedBy ECO_0000203 NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_provenance.
- befree-2016 importedOn "2016-02-19" NP553187.RAHnN-3cZd31MGte7AmAwZd1eo6LCjDPfaNX9PlV7bXSM130_provenance.