Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_provenance.
- NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_assertion wasGeneratedBy ECO_0000203 NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_provenance.
- NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_assertion wasDerivedFrom befree-20150227 NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_provenance.
- NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_assertion SIO_000772 12732643 NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_provenance.
- NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_assertion evidence source_evidence_literature NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_provenance.
- NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_assertion description "[A lethal form of nemaline myopathy, named 'Amish Nemaline Myopathy' (ANM), is linked to a nonsense mutation at codon Glu180 in the slow skeletal muscle troponin T (TnT) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977351.RABpRxosGye5iKN2WG_Yui_DVu3vcDD0CSbxbXj6p1O2g130_provenance.