Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance.
- NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_assertion description "[Identification of a common PEX1 mutation in Zellweger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance.
- NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_assertion evidence source_evidence_literature NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance.
- NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_assertion SIO_000772 10447258 NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance.
- NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_assertion wasDerivedFrom befree-2016 NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance.
- NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_assertion wasGeneratedBy ECO_0000203 NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance.
- befree-2016 importedOn "2016-02-19" NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance.