Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_provenance.
- NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_assertion description "[Mutations in the connexin 26 (Cx26) or gap junction beta 2 gene are the leading cause of hereditary nonsyndromic sensorineural hearing loss in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_provenance.
- NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_assertion evidence source_evidence_literature NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_provenance.
- NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_assertion SIO_000772 15064611 NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_provenance.
- NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_assertion wasDerivedFrom befree-20150227 NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_provenance.
- NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_assertion wasGeneratedBy ECO_0000203 NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_provenance.