Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_provenance.
- NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_assertion wasGeneratedBy ECO_0000203 NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_provenance.
- NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_assertion wasDerivedFrom befree-20150227 NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_provenance.
- NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_assertion SIO_000772 17262014 NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_provenance.
- NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_assertion evidence source_evidence_literature NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_provenance.
- NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_assertion description "[Genetic analysis of two Indian families affected with congenital hereditary endothelial dystrophy: two novel mutations in SLC4A11.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP954028.RAL1mdPj_MQZGMOafiZe0YTxmOAt-z4prYRVqhoUm0dPE130_provenance.