Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_provenance.
- NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_assertion description "[Two patients who experienced syncopes before the age of 7 years were homozygous carriers, suggesting a complete absence of calsequestrin 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_provenance.
- NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_assertion evidence source_evidence_literature NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_provenance.
- NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_assertion SIO_000772 12386154 NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_provenance.
- NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_assertion wasDerivedFrom befree-20140225 NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_provenance.
- NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_assertion wasGeneratedBy ECO_0000203 NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP348413.RAMqH76egoM09lmBg5no96LhmnHnFcinTezHQ0vB7zZ6c130_provenance.