Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_provenance.
- NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_assertion description "[We also speculate about the role of a silent mutation in exon 2 of this same gene (A45A), present in a homozygous state in the patient with both MEN2A and HSCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_provenance.
- NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_assertion evidence source_evidence_literature NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_provenance.
- NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_assertion SIO_000772 9745455 NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_provenance.
- NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_assertion wasDerivedFrom befree-2016 NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_provenance.
- NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_assertion wasGeneratedBy ECO_0000203 NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1404353.RAZcfmgRpG3T53RFYON8UasgHHOUg5v0wsKBg6LIX0JXw130_provenance.