Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_provenance.
- befree-2016 importedOn "2016-02-19" NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_provenance.
- NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_assertion wasGeneratedBy ECO_0000203 NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_provenance.
- NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_assertion wasDerivedFrom befree-2016 NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_provenance.
- NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_assertion SIO_000772 1674696 NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_provenance.
- NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_assertion evidence source_evidence_literature NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_provenance.
- NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_assertion description "[One of the five insertions was larger than that described previously, suggesting that the individuals with these mutations are unlikely to be all lineally related and that insertions in the PrP gene may not be uncommon in prion diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552841.RAKNTXIuibVI7MUkqQ-6mN96W2cJzkh94Djw7HYmpFfx8130_provenance.