Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_assertion> ?p ?o ?g. }
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- NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_assertion type Assertion NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_head.
- NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_assertion description "[We performed STRA6 molecular analysis in three fetuses and one child diagnosed with Matthew-Wood syndrome and in three siblings where two adult living brothers are affected with combinations of clinical anophthalmia, tetralogy of Fallot, and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_provenance.
- NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_assertion evidence source_evidence_literature NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_provenance.
- NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_assertion SIO_000772 19309693 NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_provenance.
- NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_assertion wasDerivedFrom befree-20140225 NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_provenance.
- NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_assertion wasGeneratedBy ECO_0000203 NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_provenance.