Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_provenance.
- NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_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." NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_provenance.
- NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_assertion evidence source_evidence_literature NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_provenance.
- NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_assertion SIO_000772 21480433 NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_provenance.
- NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_assertion wasDerivedFrom befree-20140225 NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_provenance.
- NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_assertion wasGeneratedBy ECO_0000203 NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP930688.RAj0yryKoekkaeOB0modWF0p2e0yLcY8s3zhSIeAnh8G8130_provenance.