Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_provenance.
- NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_assertion description "[The teenage sister of the proband is a carrier of the same LAMP2 mutation and has HCM without skeletal myopathy or WPW.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_provenance.
- NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_assertion evidence source_evidence_literature NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_provenance.
- NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_assertion SIO_000772 16144992 NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_provenance.
- NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_assertion wasDerivedFrom befree-20150227 NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_provenance.
- NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_assertion wasGeneratedBy ECO_0000203 NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP531425.RAcf4FDilJGlekLK41A_VwT3G9j4N3rlzdoQfCaJ4EKSs130_provenance.