Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_assertion> ?p ?o ?g. }
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- NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_assertion type Assertion NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_head.
- NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_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." NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_provenance.
- NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_assertion evidence source_evidence_literature NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_provenance.
- NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_assertion SIO_000772 18440889 NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_provenance.
- NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_assertion wasDerivedFrom befree-20150227 NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_provenance.
- NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_assertion wasGeneratedBy ECO_0000203 NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_provenance.