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- source_evidence_literature type ECO_0000212 NP1245815.RABtGVnXnPXkTMKQWNah_Mj2h2_7BjwQjr2bZ0Ft7UrRc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1245815.RABtGVnXnPXkTMKQWNah_Mj2h2_7BjwQjr2bZ0Ft7UrRc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1245815.RABtGVnXnPXkTMKQWNah_Mj2h2_7BjwQjr2bZ0Ft7UrRc130_provenance.
- NP1245815.RABtGVnXnPXkTMKQWNah_Mj2h2_7BjwQjr2bZ0Ft7UrRc130_assertion description "[De novo mutations of DYNC1H1 have been found in individuals with autosomal dominant mental retardation with neuronal migration defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245815.RABtGVnXnPXkTMKQWNah_Mj2h2_7BjwQjr2bZ0Ft7UrRc130_provenance.
- NP1245815.RABtGVnXnPXkTMKQWNah_Mj2h2_7BjwQjr2bZ0Ft7UrRc130_assertion evidence source_evidence_literature NP1245815.RABtGVnXnPXkTMKQWNah_Mj2h2_7BjwQjr2bZ0Ft7UrRc130_provenance.
- NP1245815.RABtGVnXnPXkTMKQWNah_Mj2h2_7BjwQjr2bZ0Ft7UrRc130_assertion SIO_000772 25484024 NP1245815.RABtGVnXnPXkTMKQWNah_Mj2h2_7BjwQjr2bZ0Ft7UrRc130_provenance.
- NP1245815.RABtGVnXnPXkTMKQWNah_Mj2h2_7BjwQjr2bZ0Ft7UrRc130_assertion wasDerivedFrom befree-2016 NP1245815.RABtGVnXnPXkTMKQWNah_Mj2h2_7BjwQjr2bZ0Ft7UrRc130_provenance.
- NP1245815.RABtGVnXnPXkTMKQWNah_Mj2h2_7BjwQjr2bZ0Ft7UrRc130_assertion wasGeneratedBy ECO_0000203 NP1245815.RABtGVnXnPXkTMKQWNah_Mj2h2_7BjwQjr2bZ0Ft7UrRc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1245815.RABtGVnXnPXkTMKQWNah_Mj2h2_7BjwQjr2bZ0Ft7UrRc130_provenance.