Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP771822.RAGrIWK2JCl3so7n_P0kuBIalgqWWcWrMV-H1-kDsWUCA130_provenance.