Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_provenance.
- NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_assertion description "[in hereditary hemorrhagic telangiectasia all 4 ENG mutations and one of the ACVRL1 mutations were new and had not been described previously in other populations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_provenance.
- NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_assertion evidence source_evidence_literature NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_provenance.
- NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_assertion SIO_000772 18607909 NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_provenance.
- NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_assertion wasDerivedFrom lhgdn-20090331 NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_provenance.
- NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_assertion wasGeneratedBy ECO_0000203 NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP152703.RANcNEyK20DBufZ1Y9XogsR43XrtuGHuvvJ2CdTzHzg_o130_provenance.