Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_provenance.
- NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_assertion wasGeneratedBy ECO_0000203 NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_provenance.
- NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_assertion wasDerivedFrom befree-20140225 NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_provenance.
- NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_assertion SIO_000772 14685826 NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_provenance.
- NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_assertion evidence source_evidence_literature NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_provenance.
- NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_assertion description "[Alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency (Schindler/Kanzaki disease) is a clinically and pathologically heterogeneous genetic disease with a wide spectrum including an early onset neuroaxonal dystrophy (Schindler disease) and late onset angiokeratoma corporis diffusum (Kanzaki disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP736515.RAe26doT5cx1Z53VxTvKXNVKDcxnrnjdMSdnU8BCU-_Gw130_provenance.