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- NP656337.RAXdBMR5yJyd_M9WJFQsa7gqw9CA_b-9KAen5tgmleLEE130_assertion type Assertion NP656337.RAXdBMR5yJyd_M9WJFQsa7gqw9CA_b-9KAen5tgmleLEE130_head.
- NP656337.RAXdBMR5yJyd_M9WJFQsa7gqw9CA_b-9KAen5tgmleLEE130_assertion wasGeneratedBy ECO_0000203 NP656337.RAXdBMR5yJyd_M9WJFQsa7gqw9CA_b-9KAen5tgmleLEE130_provenance.
- NP656337.RAXdBMR5yJyd_M9WJFQsa7gqw9CA_b-9KAen5tgmleLEE130_assertion wasDerivedFrom befree-2016 NP656337.RAXdBMR5yJyd_M9WJFQsa7gqw9CA_b-9KAen5tgmleLEE130_provenance.
- NP656337.RAXdBMR5yJyd_M9WJFQsa7gqw9CA_b-9KAen5tgmleLEE130_assertion SIO_000772 18285834 NP656337.RAXdBMR5yJyd_M9WJFQsa7gqw9CA_b-9KAen5tgmleLEE130_provenance.
- NP656337.RAXdBMR5yJyd_M9WJFQsa7gqw9CA_b-9KAen5tgmleLEE130_assertion evidence source_evidence_literature NP656337.RAXdBMR5yJyd_M9WJFQsa7gqw9CA_b-9KAen5tgmleLEE130_provenance.
- NP656337.RAXdBMR5yJyd_M9WJFQsa7gqw9CA_b-9KAen5tgmleLEE130_assertion description "[Indeed, one of these patients was also carrying a missense mutation in KAL1, the gene responsible for the X chromosome-linked form of Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP656337.RAXdBMR5yJyd_M9WJFQsa7gqw9CA_b-9KAen5tgmleLEE130_provenance.