Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_provenance.
- NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_assertion description "[In a population-based study from Western Sweden MLPA was used to determine the copy-numbers of several genes in the SMA region (SMN1, SMN2, BIRC1, GTF2H2 and SERF1A) in SMA-patients and their parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_provenance.
- NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_assertion evidence source_evidence_literature NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_provenance.
- NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_assertion SIO_000772 19154529 NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_provenance.
- NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_assertion wasDerivedFrom befree-20140225 NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_provenance.
- NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_assertion wasGeneratedBy ECO_0000203 NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP899869.RAESmZHAcJPZ36GrF3cXs6RNQus92r47TVwS0ONiB326Y130_provenance.