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- source_evidence_literature type ECO_0000212 NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP203890.RAMwcTor6TahRLKbzBxUDvNXaHR_jX3CM-ZcwJFlgbtzQ130_provenance.
- 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.