Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_provenance.
- NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_assertion description "[Furthermore, PRRT2 mutations elicit pleiotropy in terms of both age of expression (infancy versus later childhood) and anatomical substrate (cortex versus basal ganglia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_provenance.
- NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_assertion evidence source_evidence_literature NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_provenance.
- NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_assertion SIO_000772 22243967 NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_provenance.
- NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_assertion wasDerivedFrom befree-20140225 NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_provenance.
- NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_assertion wasGeneratedBy ECO_0000203 NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP773490.RAhVe4YPtHQtJIlWttRTHXj5V_YQuWguKns_QYzQwTdw8130_provenance.