Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance.
- NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_assertion description "[Many of the mutations known to cause either syndromic or nonsyndromic deafness occur in genes that interact with actin (e.g., the myosins, espin, and harmonin).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance.
- NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_assertion evidence source_evidence_literature NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance.
- NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_assertion SIO_000772 13680526 NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance.
- NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_assertion wasDerivedFrom befree-20140225 NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance.
- NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_assertion wasGeneratedBy ECO_0000203 NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance.