Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_provenance.
- befree-2016 importedOn "2016-02-19" NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_provenance.
- NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_assertion wasGeneratedBy ECO_0000203 NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_provenance.
- NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_assertion wasDerivedFrom befree-2016 NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_provenance.
- NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_assertion SIO_000772 22387303 NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_provenance.
- NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_assertion evidence source_evidence_literature NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_provenance.
- NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_assertion description "[Infantile neuronal ceroid lipofuscinosis (INCL; NCL1, Haltia-Santavuori disease) is caused by mutations in the CLN1/PPT gene which are associated with an early onset INCL phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP965241.RApuA_T-ogH3SA9hec_wxaSoy7iUpvIdWVxV2I7GSbDK8130_provenance.