Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_provenance.
- NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_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." NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_provenance.
- NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_assertion evidence source_evidence_literature NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_provenance.
- NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_assertion SIO_000772 12707061 NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_provenance.
- NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_assertion wasDerivedFrom befree-20140225 NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_provenance.
- NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_assertion wasGeneratedBy ECO_0000203 NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP783124.RA7w9te0pqR9jnxUKTinXKZAHHeCDlkUhu8WueEujqR1Y130_provenance.