Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_provenance.
- NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_assertion description "[Normal outcomes in neonatally ascertained siblings from index families with AGAT and GAMT deficiency suggest a potential benefit of newborn screening for these disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_provenance.
- NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_assertion evidence source_evidence_literature NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_provenance.
- NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_assertion SIO_000772 25192512 NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_provenance.
- NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_assertion wasDerivedFrom befree-2016 NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_provenance.
- NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_assertion wasGeneratedBy ECO_0000203 NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1217280.RAMN05uFmht42THoZruRkplz9DTkvpzf9fV52Qf31N-hM130_provenance.