Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_provenance.
- NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_assertion description "[Mutational analysis of the ACVRL1 gene in hereditary hemorrhagic telangiectasia patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_provenance.
- NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_assertion evidence source_evidence_literature NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_provenance.
- NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_assertion SIO_000772 15024723 NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_provenance.
- NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_assertion wasDerivedFrom lhgdn-20090331 NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_provenance.
- NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_assertion wasGeneratedBy ECO_0000203 NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP215823.RAiET1fXxV_DW92xBnclm0P-9xoULscTlP5ryZUBQpeaM130_provenance.