Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP829315.RA7aGmyMPKDWMB0wwl-HvA6A565E08bKyGoG5Q_SHTct0130_assertion> ?p ?o ?g. }
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- NP829315.RA7aGmyMPKDWMB0wwl-HvA6A565E08bKyGoG5Q_SHTct0130_assertion type Assertion NP829315.RA7aGmyMPKDWMB0wwl-HvA6A565E08bKyGoG5Q_SHTct0130_head.
- NP829315.RA7aGmyMPKDWMB0wwl-HvA6A565E08bKyGoG5Q_SHTct0130_assertion wasGeneratedBy ECO_0000203 NP829315.RA7aGmyMPKDWMB0wwl-HvA6A565E08bKyGoG5Q_SHTct0130_provenance.
- NP829315.RA7aGmyMPKDWMB0wwl-HvA6A565E08bKyGoG5Q_SHTct0130_assertion wasDerivedFrom befree-20150227 NP829315.RA7aGmyMPKDWMB0wwl-HvA6A565E08bKyGoG5Q_SHTct0130_provenance.
- NP829315.RA7aGmyMPKDWMB0wwl-HvA6A565E08bKyGoG5Q_SHTct0130_assertion SIO_000772 19822806 NP829315.RA7aGmyMPKDWMB0wwl-HvA6A565E08bKyGoG5Q_SHTct0130_provenance.
- NP829315.RA7aGmyMPKDWMB0wwl-HvA6A565E08bKyGoG5Q_SHTct0130_assertion evidence source_evidence_literature NP829315.RA7aGmyMPKDWMB0wwl-HvA6A565E08bKyGoG5Q_SHTct0130_provenance.
- NP829315.RA7aGmyMPKDWMB0wwl-HvA6A565E08bKyGoG5Q_SHTct0130_assertion description "[NOS1AP is a genetic modifier of the long-QT syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829315.RA7aGmyMPKDWMB0wwl-HvA6A565E08bKyGoG5Q_SHTct0130_provenance.