Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_provenance.
- NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_assertion description "[Dominant HEPACAM mutations can cause either macrocephaly and mental retardation with or without autism or benign familial macrocephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_provenance.
- NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_assertion evidence source_evidence_literature NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_provenance.
- NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_assertion SIO_000772 21419380 NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_provenance.
- NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_assertion wasDerivedFrom befree-20140225 NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_provenance.
- NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_assertion wasGeneratedBy ECO_0000203 NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP597901.RAuta16WkqLvKzoyJqf_k9O_VwCb3FIGvKmEEJ8QeLsQM130_provenance.