Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_provenance.
- NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_assertion wasGeneratedBy ECO_0000203 NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_provenance.
- NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_assertion wasDerivedFrom befree-20140225 NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_provenance.
- NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_assertion SIO_000772 17611253 NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_provenance.
- NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_assertion evidence source_evidence_literature NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_provenance.
- NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_assertion description "[The ACTC E101K mutation should be considered in the genetic diagnosis of LVNC, apical HCM, and septal defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP610993.RA4p6o84A3vG62FalR_xs7wRmgzXMCxbS2NIKKuAz0YvA130_provenance.