Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_provenance.
- NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_assertion wasGeneratedBy ECO_0000203 NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_provenance.
- NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_assertion wasDerivedFrom befree-2016 NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_provenance.
- NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_assertion SIO_000772 23527149 NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_provenance.
- NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_assertion evidence source_evidence_literature NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_provenance.
- NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_assertion description "[Fine mapping for Weaver syndrome in Brown Swiss cattle and the identification of 41 concordant mutations across NRCAM, PNPLA8 and CTTNBP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1063291.RAQJ6QwmZ3mD1rEsevzCLERcWL91lo2zCnS_gkLq1mUJQ130_provenance.