Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_provenance.
- NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_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." NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_provenance.
- NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_assertion evidence source_evidence_literature NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_provenance.
- NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_assertion SIO_000772 22781091 NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_provenance.
- NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_assertion wasDerivedFrom befree-2016 NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_provenance.
- NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_assertion wasGeneratedBy ECO_0000203 NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_provenance.
- befree-2016 importedOn "2016-02-19" NP996447.RARyMd_io2aWXFzlmiE2g1FohWA0CZ3LMKZrVuH0R4L4k130_provenance.