Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_provenance.
- NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_assertion description "[The association of the rare C4B3 variant with microangiopathy suggests a genetic component of its aetiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_provenance.
- NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_assertion evidence source_evidence_literature NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_provenance.
- NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_assertion SIO_000772 3926068 NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_provenance.
- NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_assertion wasDerivedFrom befree-20150227 NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_provenance.
- NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_assertion wasGeneratedBy ECO_0000203 NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1013693.RAd5Re9GAB9GkWoT0vzWRWS1LMbxbkvi0j2bpbvx9M5NM130_provenance.