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- source_evidence_literature type ECO_0000212 NP978932.RAZLpF_yrXzOaf-QbvDzCxyyGXrzD-wBW5WUz0z-9Owr4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978932.RAZLpF_yrXzOaf-QbvDzCxyyGXrzD-wBW5WUz0z-9Owr4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978932.RAZLpF_yrXzOaf-QbvDzCxyyGXrzD-wBW5WUz0z-9Owr4130_provenance.
- NP978932.RAZLpF_yrXzOaf-QbvDzCxyyGXrzD-wBW5WUz0z-9Owr4130_assertion description "[A group of 100 46,XY DSD and two POI was studied for NR5A1 mutations and their impact.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978932.RAZLpF_yrXzOaf-QbvDzCxyyGXrzD-wBW5WUz0z-9Owr4130_provenance.
- NP978932.RAZLpF_yrXzOaf-QbvDzCxyyGXrzD-wBW5WUz0z-9Owr4130_assertion evidence source_evidence_literature NP978932.RAZLpF_yrXzOaf-QbvDzCxyyGXrzD-wBW5WUz0z-9Owr4130_provenance.
- NP978932.RAZLpF_yrXzOaf-QbvDzCxyyGXrzD-wBW5WUz0z-9Owr4130_assertion SIO_000772 22549935 NP978932.RAZLpF_yrXzOaf-QbvDzCxyyGXrzD-wBW5WUz0z-9Owr4130_provenance.
- NP978932.RAZLpF_yrXzOaf-QbvDzCxyyGXrzD-wBW5WUz0z-9Owr4130_assertion wasDerivedFrom befree-2016 NP978932.RAZLpF_yrXzOaf-QbvDzCxyyGXrzD-wBW5WUz0z-9Owr4130_provenance.
- NP978932.RAZLpF_yrXzOaf-QbvDzCxyyGXrzD-wBW5WUz0z-9Owr4130_assertion wasGeneratedBy ECO_0000203 NP978932.RAZLpF_yrXzOaf-QbvDzCxyyGXrzD-wBW5WUz0z-9Owr4130_provenance.
- befree-2016 importedOn "2016-02-19" NP978932.RAZLpF_yrXzOaf-QbvDzCxyyGXrzD-wBW5WUz0z-9Owr4130_provenance.