Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_provenance.
- NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_assertion description "[In a second cross-sectional study, 1318 unrelated anonymous samples collected in 2003-2007 from patients with a broad range of signs typically found in neurofibromatosis type 1 (NF1) but no detectable NF1 germline mutation underwent SPRED1 mutation analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_provenance.
- NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_assertion evidence source_evidence_literature NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_provenance.
- NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_assertion SIO_000772 19920235 NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_provenance.
- NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_assertion wasDerivedFrom befree-2016 NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_provenance.
- NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_assertion wasGeneratedBy ECO_0000203 NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_provenance.
- befree-2016 importedOn "2016-02-19" NP776357.RARG5WJEtK6WARYglvaA5eHFTfRM4Gjc1fM5d98FjEDbU130_provenance.