Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_provenance.
- NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_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." NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_provenance.
- NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_assertion evidence source_evidence_literature NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_provenance.
- NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_assertion SIO_000772 8661155 NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_provenance.
- NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_assertion wasDerivedFrom befree-20150227 NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_provenance.
- NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_assertion wasGeneratedBy ECO_0000203 NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP699647.RAXSla82eV1huSTwAGmkuhGCUJZvXOzy967FfpvHHYKBU130_provenance.