Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_provenance.
- NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_assertion description "[Citrullinaemia is a human inborn error of metabolism resulting from the deficiency of argininosuccinate synthetase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_provenance.
- NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_assertion evidence source_evidence_literature NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_provenance.
- NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_assertion SIO_000772 6823333 NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_provenance.
- NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_assertion wasDerivedFrom befree-20150227 NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_provenance.
- NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_assertion wasGeneratedBy ECO_0000203 NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP254133.RAW5PVPz-ocm5xASgPqNzPXfNVLQFhCv2j1njvCTDdbZE130_provenance.