Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_provenance.
- NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_assertion description "[Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_provenance.
- NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_assertion evidence source_evidence_curated NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_provenance.
- NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_assertion SIO_000772 20577567 NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_provenance.
- NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_assertion wasDerivedFrom ctd_human-20150221 NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_provenance.
- NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_assertion wasGeneratedBy ECO_0000218 NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP27886.RAGwc3oLNC7m2hMZcMsXIv-dLRB5FMpmy_BvMH1Jn0PAQ130_provenance.