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- NP796079.RAiKJkCkx49VnRzNRMmLYmGHkzWDSYkBZL-g_Aa-cRKWc130_assertion type Assertion NP796079.RAiKJkCkx49VnRzNRMmLYmGHkzWDSYkBZL-g_Aa-cRKWc130_head.
- NP796079.RAiKJkCkx49VnRzNRMmLYmGHkzWDSYkBZL-g_Aa-cRKWc130_assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796079.RAiKJkCkx49VnRzNRMmLYmGHkzWDSYkBZL-g_Aa-cRKWc130_provenance.
- NP796079.RAiKJkCkx49VnRzNRMmLYmGHkzWDSYkBZL-g_Aa-cRKWc130_assertion evidence source_evidence_literature NP796079.RAiKJkCkx49VnRzNRMmLYmGHkzWDSYkBZL-g_Aa-cRKWc130_provenance.
- NP796079.RAiKJkCkx49VnRzNRMmLYmGHkzWDSYkBZL-g_Aa-cRKWc130_assertion SIO_000772 18476955 NP796079.RAiKJkCkx49VnRzNRMmLYmGHkzWDSYkBZL-g_Aa-cRKWc130_provenance.
- NP796079.RAiKJkCkx49VnRzNRMmLYmGHkzWDSYkBZL-g_Aa-cRKWc130_assertion wasDerivedFrom befree-20140225 NP796079.RAiKJkCkx49VnRzNRMmLYmGHkzWDSYkBZL-g_Aa-cRKWc130_provenance.
- NP796079.RAiKJkCkx49VnRzNRMmLYmGHkzWDSYkBZL-g_Aa-cRKWc130_assertion wasGeneratedBy ECO_0000203 NP796079.RAiKJkCkx49VnRzNRMmLYmGHkzWDSYkBZL-g_Aa-cRKWc130_provenance.