Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_provenance.
- NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_assertion description "[Finally, recent studies have disclosed plectin mutations in patients with EB with pyloric atresia, an autosomal recessive syndrome, frequently with lethal consequences.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_provenance.
- NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_assertion evidence source_evidence_literature NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_provenance.
- NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_assertion SIO_000772 15810881 NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_provenance.
- NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_assertion wasDerivedFrom befree-20140225 NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_provenance.
- NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_assertion wasGeneratedBy ECO_0000203 NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212222.RAP26FSSXBu5CfvuyZLLsB-9_DAiOT9TVqSvuuNz2rLNA130_provenance.