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- source_evidence_literature type ECO_0000212 NP333994.RA30Hew8h1D_Q2gyna_DOJaKGFbZH1CcPuoSE0cVus23Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333994.RA30Hew8h1D_Q2gyna_DOJaKGFbZH1CcPuoSE0cVus23Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333994.RA30Hew8h1D_Q2gyna_DOJaKGFbZH1CcPuoSE0cVus23Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP333994.RA30Hew8h1D_Q2gyna_DOJaKGFbZH1CcPuoSE0cVus23Q130_provenance.
- NP333994.RA30Hew8h1D_Q2gyna_DOJaKGFbZH1CcPuoSE0cVus23Q130_assertion wasGeneratedBy ECO_0000203 NP333994.RA30Hew8h1D_Q2gyna_DOJaKGFbZH1CcPuoSE0cVus23Q130_provenance.
- NP333994.RA30Hew8h1D_Q2gyna_DOJaKGFbZH1CcPuoSE0cVus23Q130_assertion wasDerivedFrom befree-2016 NP333994.RA30Hew8h1D_Q2gyna_DOJaKGFbZH1CcPuoSE0cVus23Q130_provenance.
- NP333994.RA30Hew8h1D_Q2gyna_DOJaKGFbZH1CcPuoSE0cVus23Q130_assertion SIO_000772 11673586 NP333994.RA30Hew8h1D_Q2gyna_DOJaKGFbZH1CcPuoSE0cVus23Q130_provenance.
- NP333994.RA30Hew8h1D_Q2gyna_DOJaKGFbZH1CcPuoSE0cVus23Q130_assertion evidence source_evidence_literature NP333994.RA30Hew8h1D_Q2gyna_DOJaKGFbZH1CcPuoSE0cVus23Q130_provenance.
- NP333994.RA30Hew8h1D_Q2gyna_DOJaKGFbZH1CcPuoSE0cVus23Q130_assertion description "[The clinical spectrum of SCO2 deficiency includes the delayed development of hypertrophic obstructive cardiomyopathy and severe neurogenic muscular atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333994.RA30Hew8h1D_Q2gyna_DOJaKGFbZH1CcPuoSE0cVus23Q130_provenance.