Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_provenance.
- NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_assertion description "[Three patients with SOD had heterozygous mutations in FGFR1; these were either shown to alter receptor signaling (p.S450F, p.P483S) or predicted to affect splicing (c.336C>T, p.T112T).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_provenance.
- NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_assertion evidence source_evidence_literature NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_provenance.
- NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_assertion SIO_000772 22319038 NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_provenance.
- NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_assertion wasDerivedFrom befree-2016 NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_provenance.
- NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_assertion wasGeneratedBy ECO_0000203 NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP959592.RAgOq4n3IPANppefiZ_cNpD4elfj7Lq3_Lb7KnxfLrt1Q130_provenance.