Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_provenance.
- NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_assertion description "[Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal dominant peripheral neuropathy characterized by recurrent episodes of nerve palsies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_provenance.
- NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_assertion evidence source_evidence_literature NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_provenance.
- NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_assertion SIO_000772 8565626 NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_provenance.
- NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_assertion wasDerivedFrom befree-20140225 NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_provenance.
- NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_assertion wasGeneratedBy ECO_0000203 NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP774714.RAUe3OLi_Ep7yKZdi7oEldCYjbRw_cqXFwwwIsvGCRVxo130_provenance.