Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_provenance.
- NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_assertion description "[These findings demonstrate that the spectrum of LAMB2-associated disorders is broader than previously anticipated and includes congenital nephrotic syndrome without eye anomalies or with minor ocular changes different from those observed in Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_provenance.
- NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_assertion evidence source_evidence_literature NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_provenance.
- NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_assertion SIO_000772 16912710 NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_provenance.
- NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_assertion wasDerivedFrom befree-2016 NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_provenance.
- NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_assertion wasGeneratedBy ECO_0000203 NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_provenance.
- befree-2016 importedOn "2016-02-19" NP564564.RADrBLDQ-nm2wUN9L5QXlqQlmDgxdqvvSwtf0S2vU6OYI130_provenance.