Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_provenance.
- NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_assertion description "[Comparison of aggregated clinical features in patients with or without a SPRED1 or NF1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_provenance.
- NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_assertion evidence source_evidence_literature NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_provenance.
- NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_assertion SIO_000772 19920235 NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_provenance.
- NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_assertion wasDerivedFrom befree-20140225 NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_provenance.
- NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_assertion wasGeneratedBy ECO_0000203 NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP792740.RAcQAkHJSpXgcPLH6E2SKuM-MUlQQEXS2U7LYpzo9ZOyE130_provenance.