Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_provenance.
- NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_assertion description "[For BPI only, the most interesting result was obtained for chromosome 7p21.1-p22.2 under a recessive model of inheritance (heterogeneity LOD score = 2.80), a region that had previously been linked to BP in a study on Portuguese Island families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_provenance.
- NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_assertion evidence source_evidence_literature NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_provenance.
- NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_assertion SIO_000772 21071953 NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_provenance.
- NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_assertion wasDerivedFrom befree-20140225 NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_provenance.
- NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_assertion wasGeneratedBy ECO_0000203 NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP758067.RAa2HrKfiMUre2CbLP53ZPObr24yRAlSGRJX70o5wCAX8130_provenance.