Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP323432.RASf4YCKCGTNvfTEIQkIW_2_a9e-7hbe_hur3LgHPiVNo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP323432.RASf4YCKCGTNvfTEIQkIW_2_a9e-7hbe_hur3LgHPiVNo130_assertion type Assertion NP323432.RASf4YCKCGTNvfTEIQkIW_2_a9e-7hbe_hur3LgHPiVNo130_head.
- NP323432.RASf4YCKCGTNvfTEIQkIW_2_a9e-7hbe_hur3LgHPiVNo130_assertion description "[Blau syndrome, a rare autosomal dominant genodermatosis caused by mutations in the NOD2 (nucleotide-binding oligomerization domain 2) gene, has been considered as the familial form of early-onset sarcoidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323432.RASf4YCKCGTNvfTEIQkIW_2_a9e-7hbe_hur3LgHPiVNo130_provenance.
- NP323432.RASf4YCKCGTNvfTEIQkIW_2_a9e-7hbe_hur3LgHPiVNo130_assertion evidence source_evidence_literature NP323432.RASf4YCKCGTNvfTEIQkIW_2_a9e-7hbe_hur3LgHPiVNo130_provenance.
- NP323432.RASf4YCKCGTNvfTEIQkIW_2_a9e-7hbe_hur3LgHPiVNo130_assertion SIO_000772 17372104 NP323432.RASf4YCKCGTNvfTEIQkIW_2_a9e-7hbe_hur3LgHPiVNo130_provenance.
- NP323432.RASf4YCKCGTNvfTEIQkIW_2_a9e-7hbe_hur3LgHPiVNo130_assertion wasDerivedFrom befree-20140225 NP323432.RASf4YCKCGTNvfTEIQkIW_2_a9e-7hbe_hur3LgHPiVNo130_provenance.
- NP323432.RASf4YCKCGTNvfTEIQkIW_2_a9e-7hbe_hur3LgHPiVNo130_assertion wasGeneratedBy ECO_0000203 NP323432.RASf4YCKCGTNvfTEIQkIW_2_a9e-7hbe_hur3LgHPiVNo130_provenance.