Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_provenance.
- NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_assertion description "[Therefore, implementation of systematic screening of MECP2 in MR patients should result in significant progress in the field of molecular diagnosis and genetic counseling of mental handicap.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_provenance.
- NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_assertion evidence source_evidence_literature NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_provenance.
- NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_assertion SIO_000772 11309367 NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_provenance.
- NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_assertion wasDerivedFrom befree-2016 NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_provenance.
- NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_assertion wasGeneratedBy ECO_0000203 NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_provenance.
- befree-2016 importedOn "2016-02-19" NP314935.RA3_mU1gF4GBsYN_0nC2IzUfRFtJDUh7fraZUfvvYwPYM130_provenance.