Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_assertion> ?p ?o ?g. }
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- NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_assertion type Assertion NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_head.
- NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_assertion description "[Mutations in 2 of these genes were shown to cause BFNC (KCNQ3) and hereditary deafness (KCNQ4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_provenance.
- NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_assertion evidence source_evidence_literature NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_provenance.
- NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_assertion SIO_000772 12707061 NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_provenance.
- NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_assertion wasDerivedFrom befree-20150227 NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_provenance.
- NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_assertion wasGeneratedBy ECO_0000203 NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_provenance.