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- source_evidence_literature type ECO_0000212 NP1246521.RAJHpxYxpRaal0NNwb-zgwzlAD5R4JbyBRRdkIRECsYzA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246521.RAJHpxYxpRaal0NNwb-zgwzlAD5R4JbyBRRdkIRECsYzA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246521.RAJHpxYxpRaal0NNwb-zgwzlAD5R4JbyBRRdkIRECsYzA130_provenance.
- NP1246521.RAJHpxYxpRaal0NNwb-zgwzlAD5R4JbyBRRdkIRECsYzA130_assertion description "[Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French Severe Congenital Neutropenia Registry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246521.RAJHpxYxpRaal0NNwb-zgwzlAD5R4JbyBRRdkIRECsYzA130_provenance.
- NP1246521.RAJHpxYxpRaal0NNwb-zgwzlAD5R4JbyBRRdkIRECsYzA130_assertion evidence source_evidence_literature NP1246521.RAJHpxYxpRaal0NNwb-zgwzlAD5R4JbyBRRdkIRECsYzA130_provenance.
- NP1246521.RAJHpxYxpRaal0NNwb-zgwzlAD5R4JbyBRRdkIRECsYzA130_assertion SIO_000772 25491320 NP1246521.RAJHpxYxpRaal0NNwb-zgwzlAD5R4JbyBRRdkIRECsYzA130_provenance.
- NP1246521.RAJHpxYxpRaal0NNwb-zgwzlAD5R4JbyBRRdkIRECsYzA130_assertion wasDerivedFrom befree-2016 NP1246521.RAJHpxYxpRaal0NNwb-zgwzlAD5R4JbyBRRdkIRECsYzA130_provenance.
- NP1246521.RAJHpxYxpRaal0NNwb-zgwzlAD5R4JbyBRRdkIRECsYzA130_assertion wasGeneratedBy ECO_0000203 NP1246521.RAJHpxYxpRaal0NNwb-zgwzlAD5R4JbyBRRdkIRECsYzA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246521.RAJHpxYxpRaal0NNwb-zgwzlAD5R4JbyBRRdkIRECsYzA130_provenance.