Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_provenance.
- NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_assertion description "[Phenotypic variability of cardiovascular manifestations in Marfan Syndrome. Possible role of hyperhomocysteinemia and C677T MTHFR gene polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_provenance.
- NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_assertion evidence source_evidence_literature NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_provenance.
- NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_assertion SIO_000772 14613740 NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_provenance.
- NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_assertion wasDerivedFrom gad-20150221 NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_provenance.
- NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_assertion wasGeneratedBy ECO_0000203 NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP130862.RA9eLsFmF-zduFgBT5_eB4V6r5CFhK5cGxiqQRWkcxXDg130_provenance.