Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_provenance.
- NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_assertion description "[Recurrent generalized seizures, visual loss, and palinopsia as phenotypic features of neuronal ceroid lipofuscinosis due to progranulin gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_provenance.
- NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_assertion evidence source_evidence_literature NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_provenance.
- NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_assertion SIO_000772 24779634 NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_provenance.
- NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_assertion wasDerivedFrom befree-20150227 NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_provenance.
- NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_assertion wasGeneratedBy ECO_0000203 NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434069.RADqnkZb9ICififnSqO2fMDRYlk4Uf391cX8heELyW7KI130_provenance.