Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_provenance.
- NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_assertion description "[The PPCRA phenotype is associated with a Val162Met mutation in CRB1 which is likely to affect the structure of the CRB1 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_provenance.
- NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_assertion evidence source_evidence_literature NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_provenance.
- NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_assertion SIO_000772 15623792 NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_provenance.
- NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_assertion wasDerivedFrom befree-20140225 NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_provenance.
- NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_assertion wasGeneratedBy ECO_0000203 NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP707306.RAEy1akuqMLm7VpPnwvOw8MN7ZRzSpOH4lOcD2gkBxX2Q130_provenance.