Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_provenance.
- NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_assertion description "[The cystatin C gene (CST3) encodes a low-molecular-weight cysteine proteinase inhibitor belonging to family II of the cystatin superfamily and is mutated in cases of hereditary cystatin C amyloid angiopathy (HCCAA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_provenance.
- NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_assertion evidence source_evidence_literature NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_provenance.
- NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_assertion SIO_000772 8486384 NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_provenance.
- NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_assertion wasDerivedFrom befree-20150227 NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_provenance.
- NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_assertion wasGeneratedBy ECO_0000203 NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP333383.RAB7mwTfdX_gGDLsGHE7lQgcO30n_kJ7h4onNl7E9SAHc130_provenance.