Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_provenance.
- NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_assertion description "[The structure of human alpha-GAL brings Fabry disease into the realm of molecular diseases, where insights into the structural basis of the disease phenotypes might help guide the clinical treatment of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_provenance.
- NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_assertion evidence source_evidence_literature NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_provenance.
- NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_assertion SIO_000772 15003450 NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_provenance.
- NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_assertion wasDerivedFrom befree-20150227 NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_provenance.
- NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_assertion wasGeneratedBy ECO_0000203 NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP901014.RAIO0WteI3gOeye6qlnQkr2JcQ6w3sQoFKzTkVg7yLX_g130_provenance.