Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_provenance.
- befree-2016 importedOn "2016-02-19" NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_provenance.
- NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_assertion wasGeneratedBy ECO_0000203 NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_provenance.
- NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_assertion wasDerivedFrom befree-2016 NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_provenance.
- NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_assertion SIO_000772 11565064 NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_provenance.
- NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_assertion evidence source_evidence_literature NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_provenance.
- NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_assertion description "[The results show that mutations in COL9A1 can cause MED, but they also suggest that mutations in COL9A1, COL9A2, COL9A3, COMP, and DTDST are not the major causes of MED and that there exists at least one additional locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330737.RACYO47ZQCQUwYXAJRqEhFTzFfcM5Q_r_hcZ7iSsuXjLo130_provenance.