Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_provenance.
- NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_assertion description "[Merosin (laminin-2 and -4; alpha 2-beta 1/beta 2-gamma 1) is the predominant laminin variant in skeletal muscle basement membranes; genetic defects affecting its structure or expression are the causes of some types of congenital muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_provenance.
- NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_assertion evidence source_evidence_literature NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_provenance.
- NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_assertion SIO_000772 8830776 NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_provenance.
- NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_assertion wasDerivedFrom befree-20150227 NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_provenance.
- NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_assertion wasGeneratedBy ECO_0000203 NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_provenance.