Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_provenance.
- NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_assertion description "[This is the second known instance of a male infant with omphalocele and this skeletal dysplasia born to a woman with MNS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_provenance.
- NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_assertion evidence source_evidence_literature NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_provenance.
- NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_assertion SIO_000772 7158644 NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_provenance.
- NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_assertion wasDerivedFrom befree-20150227 NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_provenance.
- NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_assertion wasGeneratedBy ECO_0000203 NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP406926.RAXVt-tm2S2aCW9H0ASuR3g13HQW1nIWi_0NtBLn69l-E130_provenance.