Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_provenance.
- NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_assertion wasGeneratedBy ECO_0000203 NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_provenance.
- NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_assertion wasDerivedFrom befree-20140225 NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_provenance.
- NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_assertion SIO_000772 11134108 NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_provenance.
- NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_assertion evidence source_evidence_literature NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_provenance.
- NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_assertion description "[This phenotypic feature is not normally associated with CPHD resulting from PROP1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP246697.RAsRS-VjkZ_lVyJ1jFgu4oANXLG0_ZZNccBsiG9_wORAk130_provenance.