Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_assertion type Assertion NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_head.
- NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_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." NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_provenance.
- NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_assertion evidence source_evidence_literature NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_provenance.
- NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_assertion SIO_000772 18476955 NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_provenance.
- NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_assertion wasDerivedFrom befree-20150227 NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_provenance.
- NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_assertion wasGeneratedBy ECO_0000203 NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_provenance.