Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_provenance.
- NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_assertion wasGeneratedBy ECO_0000203 NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_provenance.
- NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_assertion wasDerivedFrom befree-20140225 NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_provenance.
- NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_assertion SIO_000772 11297579 NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_provenance.
- NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_assertion evidence source_evidence_literature NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_provenance.
- NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_assertion description "[We examined 101 individuals with IHH (+/- anosmia) and their families to determine their modes of inheritance, incidence of mutations in the coding sequence of KAL, genotype-phenotype correlations, and [in a subset (n = 38)] their neuroendocrine phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP599814.RA49jlfuPUJUoSbMuV3He5Rp416kvgvEsZs5wXX8BWkpc130_provenance.