Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_assertion> ?p ?o ?g. }
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- NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_assertion type Assertion NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_head.
- NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.
- NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_assertion evidence source_evidence_literature NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.
- NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_assertion SIO_000772 17665217 NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.
- NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_assertion wasDerivedFrom befree-20150227 NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.
- NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_assertion wasGeneratedBy ECO_0000203 NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.