Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_provenance.
- NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_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." NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_provenance.
- NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_assertion evidence source_evidence_literature NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_provenance.
- NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_assertion SIO_000772 16859949 NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_provenance.
- NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_assertion wasDerivedFrom befree-20150227 NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_provenance.
- NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_assertion wasGeneratedBy ECO_0000203 NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP415750.RAyIWIDr3dLrlOn-Hg-J4vC-myfvyL6X8_GQV6T7IM_2c130_provenance.