Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP818756.RAByhesxEPEmVBHLJeqV9Ej4SkBrxZJqx-jX-j5QEYRqw130_provenance.