Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP634382.RAIh6qCCCgGXczqxJ2ZK02xXULqoS7PLE9SI1SuSF6Giw130_assertion> ?p ?o ?g. }
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- NP634382.RAIh6qCCCgGXczqxJ2ZK02xXULqoS7PLE9SI1SuSF6Giw130_assertion type Assertion NP634382.RAIh6qCCCgGXczqxJ2ZK02xXULqoS7PLE9SI1SuSF6Giw130_head.
- NP634382.RAIh6qCCCgGXczqxJ2ZK02xXULqoS7PLE9SI1SuSF6Giw130_assertion wasGeneratedBy ECO_0000203 NP634382.RAIh6qCCCgGXczqxJ2ZK02xXULqoS7PLE9SI1SuSF6Giw130_provenance.
- NP634382.RAIh6qCCCgGXczqxJ2ZK02xXULqoS7PLE9SI1SuSF6Giw130_assertion wasDerivedFrom befree-20140225 NP634382.RAIh6qCCCgGXczqxJ2ZK02xXULqoS7PLE9SI1SuSF6Giw130_provenance.
- NP634382.RAIh6qCCCgGXczqxJ2ZK02xXULqoS7PLE9SI1SuSF6Giw130_assertion SIO_000772 15007723 NP634382.RAIh6qCCCgGXczqxJ2ZK02xXULqoS7PLE9SI1SuSF6Giw130_provenance.
- NP634382.RAIh6qCCCgGXczqxJ2ZK02xXULqoS7PLE9SI1SuSF6Giw130_assertion evidence source_evidence_literature NP634382.RAIh6qCCCgGXczqxJ2ZK02xXULqoS7PLE9SI1SuSF6Giw130_provenance.
- NP634382.RAIh6qCCCgGXczqxJ2ZK02xXULqoS7PLE9SI1SuSF6Giw130_assertion description "[A TSC2-PKD1 contiguous gene syndrome caused by chromosomal microdeletions disrupting both the TSC2 and PKD1 genes has been identified in patients with TSC and early-onset severe ADPKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP634382.RAIh6qCCCgGXczqxJ2ZK02xXULqoS7PLE9SI1SuSF6Giw130_provenance.