Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_provenance.
- NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_assertion description "[Hereditary protein C deficiency associated with mutations in exon IX of the protein C gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_provenance.
- NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_assertion evidence source_evidence_literature NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_provenance.
- NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_assertion SIO_000772 7831652 NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_provenance.
- NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_assertion wasDerivedFrom gad-20150221 NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_provenance.
- NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_assertion wasGeneratedBy ECO_0000203 NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP65866.RAaomzsw3go189MFpOS-ixqYRkGhhd9ZDq1OLZ7KQ9KH0130_provenance.