Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_provenance.
- NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_assertion description "[De novo ASXL1 mutations cause Bohring-Opitz syndrome characterized by multiple congenital malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_provenance.
- NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_assertion evidence source_evidence_literature NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_provenance.
- NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_assertion SIO_000772 24255920 NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_provenance.
- NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_assertion wasDerivedFrom befree-2016 NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_provenance.
- NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_assertion wasGeneratedBy ECO_0000203 NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1129848.RA6Pj7sNp5aOwF53Srym5jHddp8sILC25mAeltcnLWgWY130_provenance.