Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_provenance.
- NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_assertion description "[Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_provenance.
- NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_assertion evidence source_evidence_literature NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_provenance.
- NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_assertion SIO_000772 1981052 NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_provenance.
- NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_assertion wasDerivedFrom befree-2016 NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_provenance.
- NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_assertion wasGeneratedBy ECO_0000203 NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_provenance.
- befree-2016 importedOn "2016-02-19" NP767965.RAAjhsTIjyoPk10tndr8h-yew1A1ZQrMO2yGz5SCuFDc0130_provenance.