Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_provenance.
- NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_assertion description "[To characterize the ocular phenotype resulting from mutation of Rab38, a candidate gene for Hermansky-Pudlak syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_provenance.
- NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_assertion evidence source_evidence_literature NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_provenance.
- NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_assertion SIO_000772 17724166 NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_provenance.
- NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_assertion wasDerivedFrom befree-20150227 NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_provenance.
- NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_assertion wasGeneratedBy ECO_0000203 NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP877047.RAGMIHx8bUALZSF3_VNqSCkbXqFBOG1PCu4aQgPjVAqA8130_provenance.