Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_provenance.
- NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_assertion description "[Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_provenance.
- NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_assertion evidence source_evidence_literature NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_provenance.
- NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_assertion SIO_000772 19384346 NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_provenance.
- NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_assertion wasDerivedFrom befree-2016 NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_provenance.
- NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_assertion wasGeneratedBy ECO_0000203 NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP733977.RABxkqbRjZdgzWpt7gD2NabtnQU6yvWLNkTT9H5sghCnQ130_provenance.