Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_provenance.
- NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_assertion description "[Mutations in the four main genes involved in HPE (SHH, ZIC2, SIX3, TGIF) were identified in 25% of cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_provenance.
- NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_assertion evidence source_evidence_literature NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_provenance.
- NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_assertion SIO_000772 21940735 NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_provenance.
- NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_assertion wasDerivedFrom befree-20150227 NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_provenance.
- NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_assertion wasGeneratedBy ECO_0000203 NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP693425.RAqy9KJxiWWX40NKvZVcUbn-PWCvVyFWWEFZOeBlfaoUw130_provenance.