Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_provenance.
- NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_assertion description "[Congenital heart defects in the affected relatives were discordant in the families with PTPN11 mutations, and concordant in that with RAF1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_provenance.
- NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_assertion evidence source_evidence_literature NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_provenance.
- NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_assertion SIO_000772 22781091 NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_provenance.
- NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_assertion wasDerivedFrom befree-20140225 NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_provenance.
- NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_assertion wasGeneratedBy ECO_0000203 NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_provenance.