Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_provenance.
- befree-2016 importedOn "2016-02-19" NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_provenance.
- NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_assertion wasGeneratedBy ECO_0000203 NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_provenance.
- NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_assertion wasDerivedFrom befree-2016 NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_provenance.
- NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_assertion SIO_000772 17276711 NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_provenance.
- NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_assertion evidence source_evidence_literature NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_provenance.
- NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_assertion description "[Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592199.RAGfa5a5uo1zlPPcYzYo8esv3eSiu5Guvqbe_zQkf2bPI130_provenance.