Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_provenance.
- NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_assertion description "[GLRB itself does not seem to be a good candidate as it causes autosomal recessive hyperekplexia and no symptoms were found in the patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_provenance.
- NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_assertion evidence source_evidence_literature NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_provenance.
- NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_assertion SIO_000772 22669415 NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_provenance.
- NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_assertion wasDerivedFrom befree-20150227 NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_provenance.
- NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_assertion wasGeneratedBy ECO_0000203 NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP428881.RAhWwuG167smE5e6Ue1OHR5VR4lr3MVwx0vj3J3OxusXY130_provenance.