Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_provenance.
- NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_assertion description "[Given that mutations in EFEMP1 have been recently described in patients with Doyne honeycomb retinal dystrophy, EFEMP2 becomes a good candidate for such disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_provenance.
- NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_assertion evidence source_evidence_literature NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_provenance.
- NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_assertion SIO_000772 10982184 NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_provenance.
- NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_assertion wasDerivedFrom befree-20140225 NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_provenance.
- NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_assertion wasGeneratedBy ECO_0000203 NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP646076.RAbnSca6d5jduhV1DvOWUCiHP72o72xpT-XSf4D2_0zT4130_provenance.