Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_provenance.
- NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_assertion description "[The majority of associated anomalies, with the exception of psychomotor retardation and Chiari malformation, were detected more frequently in TWIST1 patients than in FGFR3 p.P250R patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_provenance.
- NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_assertion evidence source_evidence_literature NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_provenance.
- NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_assertion SIO_000772 22544111 NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_provenance.
- NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_assertion wasDerivedFrom befree-2016 NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_provenance.
- NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_assertion wasGeneratedBy ECO_0000203 NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_provenance.
- befree-2016 importedOn "2016-02-19" NP978380.RAIWK4cHwidH78FSBo_wxx5y8JDxjGzHDtbylE1EsWgLM130_provenance.