Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_provenance.
- NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_assertion description "[The patient is heterozygous for an alteration in the A2M gene; this may be responsible for his serum A2M deficiency and may be relevant to the early onset of pulmonary disease in his case.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_provenance.
- NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_assertion evidence source_evidence_literature NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_provenance.
- NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_assertion SIO_000772 2475424 NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_provenance.
- NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_assertion wasDerivedFrom befree-20150227 NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_provenance.
- NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_assertion wasGeneratedBy ECO_0000203 NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP217226.RACwfuQ-RoxsSw3l1YgDvoTWQBZqNwaAyGkIdKBWItFX8130_provenance.