Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_provenance.
- befree-2016 importedOn "2016-02-19" NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_provenance.
- NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_assertion wasGeneratedBy ECO_0000203 NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_provenance.
- NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_assertion wasDerivedFrom befree-2016 NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_provenance.
- NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_assertion SIO_000772 19421414 NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_provenance.
- NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_assertion evidence source_evidence_literature NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_provenance.
- NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_assertion description "[Genetic variation in MTHFR does not provide an explanation for the variable phenotype in LHON.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP737074.RAyeMhC5dIdFdWJoOwV1LOHP0qRUrLZF9r2gkPCQtfK7M130_provenance.