Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP523383.RAIC_Hurpp9J9CY4Yw0KM8PWSkILp3asQXcVXTJZ0ydbw130_provenance.