Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_assertion> ?p ?o ?g. }
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- NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_assertion type Assertion NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_head.
- NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_assertion description "[Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular dysfunction (USH1D) were previously mapped to overlapping regions of chromosome 10q21-q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.
- NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_assertion evidence source_evidence_literature NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.
- NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_assertion SIO_000772 11090341 NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.
- NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_assertion wasDerivedFrom befree-20140225 NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.
- NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_assertion wasGeneratedBy ECO_0000203 NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.