Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_provenance.
- befree-2016 importedOn "2016-02-19" NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_provenance.
- NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_assertion wasGeneratedBy ECO_0000203 NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_provenance.
- NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_assertion wasDerivedFrom befree-2016 NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_provenance.
- NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_assertion SIO_000772 16510324 NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_provenance.
- NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_assertion evidence source_evidence_literature NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_provenance.
- NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_assertion description "[Fabry disease (FD) is an X-linked inborn error of metabolism resulting from the deficient activity of alpha-galactosidase A which leads to the widespread deposition of glycosphingolipids in lysosomes, and to ischemic complications involving kidneys, heart and brain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP538244.RALa21c-L0SNy_gKayH9A949SXN7OAGLY3gqUGKNLJ1-A130_provenance.