Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_provenance.
- NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_assertion description "[Branchio-oto-renal syndrome (BOR) is an autosomal dominant developmental disorder characterized by the association of branchial arch defects, hearing loss, and renal anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_provenance.
- NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_assertion evidence source_evidence_literature NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_provenance.
- NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_assertion SIO_000772 17357085 NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_provenance.
- NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_assertion wasDerivedFrom befree-20140225 NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_provenance.
- NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_assertion wasGeneratedBy ECO_0000203 NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP172465.RARvIubdQVx_V2ZqIqzq4c0C_mhKD-T2zv6V1DjUhKA4E130_provenance.