Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_provenance.
- befree-2016 importedOn "2016-02-19" NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_provenance.
- NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_assertion wasGeneratedBy ECO_0000203 NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_provenance.
- NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_assertion wasDerivedFrom befree-2016 NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_provenance.
- NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_assertion SIO_000772 11857753 NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_provenance.
- NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_assertion evidence source_evidence_literature NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_provenance.
- NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_assertion description "[In this study, we report the co-existence, in a 5-year old boy with FA, of a double mutation in two distinct genes [X25 (A allele: 850 triplets; B allele: 1000 triplets), and cardiac troponin T (TNNT2) (287G>A)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP346156.RA3IFFH879ljgh0C5pdjY7Z_rAjgt_yWLdSkAAtZv9_CI130_provenance.