Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_provenance.
- NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_assertion description "[In this study, we investigate the prevalence and phenotype/genotype correlation of connexin (CX) gene family variants in a cohort of children with nonsyndromic hearing loss (HL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_provenance.
- NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_assertion evidence source_evidence_literature NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_provenance.
- NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_assertion SIO_000772 20593197 NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_provenance.
- NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_assertion wasDerivedFrom befree-20150227 NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_provenance.
- NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_assertion wasGeneratedBy ECO_0000203 NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_provenance.