Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_assertion> ?p ?o ?g. }
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- NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_assertion type Assertion NP273808.RAp-QfTv3cISRX4h_EmXuxJ-eQnfvDXA0HB4tld2zgl8U130_head.
- 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.