Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance.
- NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_assertion description "[Congenital muscular dystrophy with dropped head phenotype and cognitive impairment due to a novel mutation in the LMNA gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance.
- NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_assertion evidence source_evidence_literature NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance.
- NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_assertion SIO_000772 24684859 NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance.
- NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_assertion wasDerivedFrom befree-20150227 NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance.
- NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_assertion wasGeneratedBy ECO_0000203 NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP537782.RAKzkrvjSGgXqFmKjuSo8lhe8cbgcQkY2GMDVvsDl4izY130_provenance.