Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP614697.RA807DMFzYwpi2a1eQfo3YsCii7vT3qd16zQzdo_ES4iM130_assertion> ?p ?o ?g. }
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- NP614697.RA807DMFzYwpi2a1eQfo3YsCii7vT3qd16zQzdo_ES4iM130_assertion type Assertion NP614697.RA807DMFzYwpi2a1eQfo3YsCii7vT3qd16zQzdo_ES4iM130_head.
- NP614697.RA807DMFzYwpi2a1eQfo3YsCii7vT3qd16zQzdo_ES4iM130_assertion description "[Mutations in the NOG gene which encodes the noggin protein, a bone morphogenetic protein antagonist, have been identified in TCS as well as in four other autosomal dominant disorders including proximal symphalangism (SYM1), multiple synostosis (SYNS1), Tarsal-Carpal coalition syndrome and brachydactyly type B (BDB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614697.RA807DMFzYwpi2a1eQfo3YsCii7vT3qd16zQzdo_ES4iM130_provenance.
- NP614697.RA807DMFzYwpi2a1eQfo3YsCii7vT3qd16zQzdo_ES4iM130_assertion evidence source_evidence_literature NP614697.RA807DMFzYwpi2a1eQfo3YsCii7vT3qd16zQzdo_ES4iM130_provenance.
- NP614697.RA807DMFzYwpi2a1eQfo3YsCii7vT3qd16zQzdo_ES4iM130_assertion SIO_000772 18440889 NP614697.RA807DMFzYwpi2a1eQfo3YsCii7vT3qd16zQzdo_ES4iM130_provenance.
- NP614697.RA807DMFzYwpi2a1eQfo3YsCii7vT3qd16zQzdo_ES4iM130_assertion wasDerivedFrom befree-20140225 NP614697.RA807DMFzYwpi2a1eQfo3YsCii7vT3qd16zQzdo_ES4iM130_provenance.
- NP614697.RA807DMFzYwpi2a1eQfo3YsCii7vT3qd16zQzdo_ES4iM130_assertion wasGeneratedBy ECO_0000203 NP614697.RA807DMFzYwpi2a1eQfo3YsCii7vT3qd16zQzdo_ES4iM130_provenance.