Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_provenance.
- NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_assertion description "[Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_provenance.
- NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_assertion evidence source_evidence_curated NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_provenance.
- NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_assertion SIO_000772 7529962 NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_provenance.
- NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_assertion wasDerivedFrom uniprot-2016 NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_provenance.
- NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_assertion wasGeneratedBy ECO_0000218 NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8312.RA113pxcMexIH1gzDeII10AyzT9KVvoD-VtwEwMniv4Bg130_provenance.