Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_provenance.
- NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_assertion description "[Mutations in the genes for endoglin (ENG) and for activin A receptor type II-like kinase 1 (ACVRL1) have been identified to cause HHT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_provenance.
- NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_assertion evidence source_evidence_curated NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_provenance.
- NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_assertion SIO_000772 16525724 NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_provenance.
- NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_assertion wasDerivedFrom uniprot-20150221 NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_provenance.
- NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_assertion wasGeneratedBy ECO_0000218 NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1801.RAnvLjGgGmDYKnMgBgKxNbaMgsF2jVKC0O7nUifvhp7wg130_provenance.