Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_provenance.
- NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_assertion description "[Recessive mutant alleles of MYO7A, USH1C, CDH23, and PCDH15 cause non-syndromic deafness or type 1 Usher syndrome (USH1) characterised by deafness, vestibular areflexia, and vision loss due to retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_provenance.
- NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_assertion evidence source_evidence_literature NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_provenance.
- NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_assertion SIO_000772 21940737 NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_provenance.
- NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_assertion wasDerivedFrom befree-2016 NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_provenance.
- NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_assertion wasGeneratedBy ECO_0000203 NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_provenance.
- befree-2016 importedOn "2016-02-19" NP925807.RATa7twa37MhYQUaTJWGLGOUe9dISb7sBTrkXcVjQyhsk130_provenance.