Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_provenance.
- befree-2016 importedOn "2016-02-19" NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_provenance.
- NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_assertion wasGeneratedBy ECO_0000203 NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_provenance.
- NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_assertion wasDerivedFrom befree-2016 NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_provenance.
- NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_assertion SIO_000772 16398470 NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_provenance.
- NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_assertion evidence source_evidence_literature NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_provenance.
- NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_assertion description "[The catalog of mutations identified thus far has facilitated extensive genetic analysis, including studies of patients with mosaicism and phenotype-genotype correlations, and has also led to experiments that have begun to unravel the molecular biology of the NF2 gene and its role in tumorigenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529937.RAegJNaijRo9gVfQC2M8NjC-zcn2aeNfZFeKh36G-FJqk130_provenance.