Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance.
- NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_assertion description "[Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance.
- NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_assertion evidence source_evidence_literature NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance.
- NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_assertion SIO_000772 7704558 NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance.
- NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_assertion wasDerivedFrom befree-20140225 NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance.
- NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_assertion wasGeneratedBy ECO_0000203 NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance.
- befree-20140225 importedOn "2014-02-25" NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance.