Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance.
- NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_assertion description "[This indel mutation in FHL1 broadens the spectrum of FHL1-related disorders and implicates it in the pathogenesis of NS spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance.
- NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_assertion evidence source_evidence_literature NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance.
- NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_assertion SIO_000772 23456229 NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance.
- NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_assertion wasDerivedFrom befree-20150227 NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance.
- NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_assertion wasGeneratedBy ECO_0000203 NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance.
- befree-20150227 importedOn "2015-02-27" NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance.