Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_assertion> ?p ?o ?g. }
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- NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_assertion type Assertion NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_head.
- NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_assertion wasGeneratedBy ECO_0000203 NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_provenance.
- NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_assertion wasDerivedFrom lhgdn-20090331 NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_provenance.
- NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_assertion SIO_000772 15001591 NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_provenance.
- NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_assertion evidence source_evidence_literature NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_provenance.
- NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_assertion description "[six novel and two recurrent intragenic KAL1 mutations in seven familial and four sporadic male cases of Kallmann syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_provenance.