Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_provenance.
- NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_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." NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_provenance.
- NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_assertion evidence source_evidence_literature NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_provenance.
- NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_assertion SIO_000772 22549935 NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_provenance.
- NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_assertion wasDerivedFrom befree-2016 NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_provenance.
- NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_assertion wasGeneratedBy ECO_0000203 NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_provenance.
- befree-2016 importedOn "2016-02-19" NP978933.RAeD_IZsO5CQ3xJ2uOP7ooMvFNcOba0jntP8l8gXAp25E130_provenance.