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- source_evidence_literature type ECO_0000212 NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.
- NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_assertion description "[We identified a c.1625G > T mutation in exon 12 of COCH that co-segregates with auditory dysfunction in the pedigree.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.
- NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_assertion evidence source_evidence_literature NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.
- NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_assertion SIO_000772 16261627 NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.
- NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_assertion wasDerivedFrom befree-2016 NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.
- NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_assertion wasGeneratedBy ECO_0000203 NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.
- befree-2016 importedOn "2016-02-19" NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.