Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_provenance.
- NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_assertion description "[In approximately 20% of cases of severe congenital neutropenia (SCN), mutations are found in the gene encoding the granulocyte colony-stimulating factor receptor (G-CSF-R).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_provenance.
- NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_assertion evidence source_evidence_literature NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_provenance.
- NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_assertion SIO_000772 9989983 NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_provenance.
- NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_assertion wasDerivedFrom befree-2016 NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_provenance.
- NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_assertion wasGeneratedBy ECO_0000203 NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1414860.RAePL5xctUz5Es3c5eGSdYO4jdp2un72fqbcE7cBbApj0130_provenance.