Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_provenance.
- NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_assertion description "[Since the creatine transporter has a prominent function in muscular physiology, it is a candidate gene for Barth syndrome and infantile cardiomyopathy mapped to Xq28.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_provenance.
- NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_assertion evidence source_evidence_literature NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_provenance.
- NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_assertion SIO_000772 8661155 NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_provenance.
- NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_assertion wasDerivedFrom befree-20140225 NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_provenance.
- NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_assertion wasGeneratedBy ECO_0000203 NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_provenance.
- befree-20140225 importedOn "2014-02-25" NP531894.RAC0-pzXx4kI47i-LhbWAYjAllEQQ2GZCPcaW-sooAr64130_provenance.