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- source_evidence_literature type ECO_0000212 NP586676.RAXTYb-KQ94WEixVF1fY6ARbb2Ro1bi9OFfwsnjkki1b0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586676.RAXTYb-KQ94WEixVF1fY6ARbb2Ro1bi9OFfwsnjkki1b0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586676.RAXTYb-KQ94WEixVF1fY6ARbb2Ro1bi9OFfwsnjkki1b0130_provenance.
- NP586676.RAXTYb-KQ94WEixVF1fY6ARbb2Ro1bi9OFfwsnjkki1b0130_assertion description "[A biochemical diagnosis of complex I deficiency on cultured amniocytes from a later pregnancy was confirmed through the identification of disease causing NDUFS3 mutations in these cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586676.RAXTYb-KQ94WEixVF1fY6ARbb2Ro1bi9OFfwsnjkki1b0130_provenance.
- NP586676.RAXTYb-KQ94WEixVF1fY6ARbb2Ro1bi9OFfwsnjkki1b0130_assertion evidence source_evidence_literature NP586676.RAXTYb-KQ94WEixVF1fY6ARbb2Ro1bi9OFfwsnjkki1b0130_provenance.
- NP586676.RAXTYb-KQ94WEixVF1fY6ARbb2Ro1bi9OFfwsnjkki1b0130_assertion SIO_000772 14729820 NP586676.RAXTYb-KQ94WEixVF1fY6ARbb2Ro1bi9OFfwsnjkki1b0130_provenance.
- NP586676.RAXTYb-KQ94WEixVF1fY6ARbb2Ro1bi9OFfwsnjkki1b0130_assertion wasDerivedFrom befree-20150227 NP586676.RAXTYb-KQ94WEixVF1fY6ARbb2Ro1bi9OFfwsnjkki1b0130_provenance.
- NP586676.RAXTYb-KQ94WEixVF1fY6ARbb2Ro1bi9OFfwsnjkki1b0130_assertion wasGeneratedBy ECO_0000203 NP586676.RAXTYb-KQ94WEixVF1fY6ARbb2Ro1bi9OFfwsnjkki1b0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP586676.RAXTYb-KQ94WEixVF1fY6ARbb2Ro1bi9OFfwsnjkki1b0130_provenance.