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- source_evidence_literature type ECO_0000212 NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_provenance.
- NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_assertion description "[Here, we identify missense mutations in the calcium channel gene CACNA1H (T-type Ca(V)3.2) in 6 of 461 individuals with ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_provenance.
- NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_assertion evidence source_evidence_literature NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_provenance.
- NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_assertion SIO_000772 16754686 NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_provenance.
- NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_assertion wasDerivedFrom befree-20150227 NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_provenance.
- NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_assertion wasGeneratedBy ECO_0000203 NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_provenance.