Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_provenance.
- NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_assertion description "[The frequencies of the host genetic factors in the whole group were 0.52 for blood group O, 0.13 for hemoglobin S, 0.16 for the G6PD A-deficient variant and 0.24 for alpha+-thalassemia (-alpha(3.7) deletion).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_provenance.
- NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_assertion evidence source_evidence_literature NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_provenance.
- NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_assertion SIO_000772 16859949 NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_provenance.
- NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_assertion wasDerivedFrom befree-2016 NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_provenance.
- NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_assertion wasGeneratedBy ECO_0000203 NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_provenance.
- befree-2016 importedOn "2016-02-19" NP560804.RAP_kssCvCx-s29IP9SI6eP8cIMFm8DwWa0KGAI4TveFs130_provenance.