Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_provenance.
- NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_assertion description "[An infant with multiple anomalies and developmental delay during his first year was found to have an intersitital deletion of band p14 from the proximal short arm of chromosome 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_provenance.
- NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_assertion evidence source_evidence_literature NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_provenance.
- NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_assertion SIO_000772 7424912 NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_provenance.
- NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_assertion wasDerivedFrom befree-20150227 NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_provenance.
- NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_assertion wasGeneratedBy ECO_0000203 NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_provenance.
- befree-20150227 importedOn "2015-02-27" NP306081.RAyoBurh5tbao_SmLYu7bpY4zBjeT9X-fnS1RBlBKW450130_provenance.