Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance.
- NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_assertion description "[Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance.
- NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_assertion evidence source_evidence_literature NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance.
- NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_assertion SIO_000772 9856479 NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance.
- NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_assertion wasDerivedFrom befree-2016 NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance.
- NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_assertion wasGeneratedBy ECO_0000203 NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance.