Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_provenance.
- NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_assertion description "[This study reports on bioinformatic and moleculardata for the FAM46A gene that may give a wider insight into the putative function of this gene and its pathologic relevance to RP25 and other retinal diseases mapping within the 6q chromosomal interval.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_provenance.
- NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_assertion evidence source_evidence_literature NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_provenance.
- NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_assertion SIO_000772 17803723 NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_provenance.
- NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_assertion wasDerivedFrom befree-20150227 NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_provenance.
- NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_assertion wasGeneratedBy ECO_0000203 NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP919325.RA-HJ9UxtgHHE3spzI_We57zOyTU-hgQZldwDjDPwHUn0130_provenance.