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- source_evidence_literature type ECO_0000212 NP537636.RA0nEOeH7sIjOM5kK9f-JfJvJilGhvusVLJnwdbQRR4IA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537636.RA0nEOeH7sIjOM5kK9f-JfJvJilGhvusVLJnwdbQRR4IA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537636.RA0nEOeH7sIjOM5kK9f-JfJvJilGhvusVLJnwdbQRR4IA130_provenance.
- NP537636.RA0nEOeH7sIjOM5kK9f-JfJvJilGhvusVLJnwdbQRR4IA130_assertion description "[Rare mutations in LMNA were recently shown to underlie familial partial lipodystrophy (FPLD), a syndrome characterized by regional loss of adipose tissue, insulin resistance, and glucose intolerance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537636.RA0nEOeH7sIjOM5kK9f-JfJvJilGhvusVLJnwdbQRR4IA130_provenance.
- NP537636.RA0nEOeH7sIjOM5kK9f-JfJvJilGhvusVLJnwdbQRR4IA130_assertion evidence source_evidence_literature NP537636.RA0nEOeH7sIjOM5kK9f-JfJvJilGhvusVLJnwdbQRR4IA130_provenance.
- NP537636.RA0nEOeH7sIjOM5kK9f-JfJvJilGhvusVLJnwdbQRR4IA130_assertion SIO_000772 11243729 NP537636.RA0nEOeH7sIjOM5kK9f-JfJvJilGhvusVLJnwdbQRR4IA130_provenance.
- NP537636.RA0nEOeH7sIjOM5kK9f-JfJvJilGhvusVLJnwdbQRR4IA130_assertion wasDerivedFrom befree-20150227 NP537636.RA0nEOeH7sIjOM5kK9f-JfJvJilGhvusVLJnwdbQRR4IA130_provenance.
- NP537636.RA0nEOeH7sIjOM5kK9f-JfJvJilGhvusVLJnwdbQRR4IA130_assertion wasGeneratedBy ECO_0000203 NP537636.RA0nEOeH7sIjOM5kK9f-JfJvJilGhvusVLJnwdbQRR4IA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP537636.RA0nEOeH7sIjOM5kK9f-JfJvJilGhvusVLJnwdbQRR4IA130_provenance.