Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_provenance.
- NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_assertion description "[Three individuals with smaller, nonrecurrent deletions (?180-500 kb) that include HIP1 but not YWHAG suggest that deletion of HIP1 is sufficient to cause neurological disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_provenance.
- NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_assertion evidence source_evidence_literature NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_provenance.
- NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_assertion SIO_000772 21109226 NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_provenance.
- NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_assertion wasDerivedFrom befree-2016 NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_provenance.
- NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_assertion wasGeneratedBy ECO_0000203 NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_provenance.
- befree-2016 importedOn "2016-02-19" NP854915.RAXC1NyAcz4MjWYFoQooebNf5OtqK0hOg3iGz8ZKpYnPc130_provenance.