Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_provenance.
- NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_assertion wasGeneratedBy ECO_0000203 NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_provenance.
- NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_assertion wasDerivedFrom befree-20140225 NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_provenance.
- NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_assertion SIO_000772 11673586 NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_provenance.
- NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_assertion evidence source_evidence_literature NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_provenance.
- NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_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." NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP404228.RA5u2pi_LICaI_DjsyQnKPK_l-8wwoGHSyIo0Bi3p_ycg130_provenance.