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- source_evidence_literature type ECO_0000212 NP886020.RA-73f7wAC4MpC9BlSQjA12Dim1H75qlVRYoMjPyH7R3k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886020.RA-73f7wAC4MpC9BlSQjA12Dim1H75qlVRYoMjPyH7R3k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP886020.RA-73f7wAC4MpC9BlSQjA12Dim1H75qlVRYoMjPyH7R3k130_provenance.
- NP886020.RA-73f7wAC4MpC9BlSQjA12Dim1H75qlVRYoMjPyH7R3k130_assertion description "[Although mutations in MYH14 have been shown to cause nonsyndromic autosomal dominant hearing loss (DFNA4), the peripheral neuropathy, myopathy, and hoarseness have not been associated with MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886020.RA-73f7wAC4MpC9BlSQjA12Dim1H75qlVRYoMjPyH7R3k130_provenance.
- NP886020.RA-73f7wAC4MpC9BlSQjA12Dim1H75qlVRYoMjPyH7R3k130_assertion evidence source_evidence_literature NP886020.RA-73f7wAC4MpC9BlSQjA12Dim1H75qlVRYoMjPyH7R3k130_provenance.
- NP886020.RA-73f7wAC4MpC9BlSQjA12Dim1H75qlVRYoMjPyH7R3k130_assertion SIO_000772 21480433 NP886020.RA-73f7wAC4MpC9BlSQjA12Dim1H75qlVRYoMjPyH7R3k130_provenance.
- NP886020.RA-73f7wAC4MpC9BlSQjA12Dim1H75qlVRYoMjPyH7R3k130_assertion wasDerivedFrom befree-2016 NP886020.RA-73f7wAC4MpC9BlSQjA12Dim1H75qlVRYoMjPyH7R3k130_provenance.
- NP886020.RA-73f7wAC4MpC9BlSQjA12Dim1H75qlVRYoMjPyH7R3k130_assertion wasGeneratedBy ECO_0000203 NP886020.RA-73f7wAC4MpC9BlSQjA12Dim1H75qlVRYoMjPyH7R3k130_provenance.
- befree-2016 importedOn "2016-02-19" NP886020.RA-73f7wAC4MpC9BlSQjA12Dim1H75qlVRYoMjPyH7R3k130_provenance.