Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_assertion type Assertion NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_head.
- NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_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." NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_provenance.
- NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_assertion evidence source_evidence_literature NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_provenance.
- NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_assertion SIO_000772 18476955 NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_provenance.
- NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_assertion wasDerivedFrom befree-20140225 NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_provenance.
- NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_assertion wasGeneratedBy ECO_0000203 NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_provenance.