Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_provenance.
- NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_assertion description "[Variants of OTOF and PJVK genes in Chinese patients with auditory neuropathy spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_provenance.
- NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_assertion evidence source_evidence_literature NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_provenance.
- NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_assertion SIO_000772 21935370 NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_provenance.
- NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_assertion wasDerivedFrom befree-2016 NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_provenance.
- NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_assertion wasGeneratedBy ECO_0000203 NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_provenance.
- befree-2016 importedOn "2016-02-19" NP925272.RAsn9m5w7yYq_qv0Ad9imP0ur5R8inbry9UfmNLiNGKig130_provenance.