Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_assertion> ?p ?o ?g. }
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- NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_assertion type Assertion NP1012310.RAmmNUnHHojC13PUjJdCBftKMnD18WS2t1IVLTdozIlbs130_head.
- 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.