Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_provenance.
- NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_assertion description "[Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_provenance.
- NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_assertion evidence source_evidence_literature NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_provenance.
- NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_assertion SIO_000772 23043934 NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_provenance.
- NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_assertion wasDerivedFrom befree-20150227 NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_provenance.
- NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_assertion wasGeneratedBy ECO_0000203 NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP577089.RAWNIpNzUSkR8LcWEV1w7uyeBk-P0eFLJ1yu_vID1dAB4130_provenance.