Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_provenance.
- NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_assertion description "[Recently, we reported mutations in the 1-acylglycerol-3-phosphate O-acyltransferase 2 (AGPAT2) gene in CGL pedigrees linked to chromosome 9q34 (CGL1 subtype), and mutations in the Seipin gene were reported in pedigrees linked to chromosome 11q13 (CGL2 subtype).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_provenance.
- NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_assertion evidence source_evidence_literature NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_provenance.
- NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_assertion SIO_000772 14602785 NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_provenance.
- NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_assertion wasDerivedFrom befree-20140225 NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_provenance.
- NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_assertion wasGeneratedBy ECO_0000203 NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP777583.RA759U0hBm46BfFCWzjqM3yfZ-ZeZm518Hn41T1dZfJR8130_provenance.