Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP473646.RAA-6NVKN5ruhURZRMZ1ggkb4iWgjUeNx4udsw7l4jy4k130_assertion> ?p ?o ?g. }
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- NP473646.RAA-6NVKN5ruhURZRMZ1ggkb4iWgjUeNx4udsw7l4jy4k130_assertion type Assertion NP473646.RAA-6NVKN5ruhURZRMZ1ggkb4iWgjUeNx4udsw7l4jy4k130_head.
- NP473646.RAA-6NVKN5ruhURZRMZ1ggkb4iWgjUeNx4udsw7l4jy4k130_assertion description "[A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP473646.RAA-6NVKN5ruhURZRMZ1ggkb4iWgjUeNx4udsw7l4jy4k130_provenance.
- NP473646.RAA-6NVKN5ruhURZRMZ1ggkb4iWgjUeNx4udsw7l4jy4k130_assertion evidence source_evidence_literature NP473646.RAA-6NVKN5ruhURZRMZ1ggkb4iWgjUeNx4udsw7l4jy4k130_provenance.
- NP473646.RAA-6NVKN5ruhURZRMZ1ggkb4iWgjUeNx4udsw7l4jy4k130_assertion SIO_000772 16735904 NP473646.RAA-6NVKN5ruhURZRMZ1ggkb4iWgjUeNx4udsw7l4jy4k130_provenance.
- NP473646.RAA-6NVKN5ruhURZRMZ1ggkb4iWgjUeNx4udsw7l4jy4k130_assertion wasDerivedFrom befree-20140225 NP473646.RAA-6NVKN5ruhURZRMZ1ggkb4iWgjUeNx4udsw7l4jy4k130_provenance.
- NP473646.RAA-6NVKN5ruhURZRMZ1ggkb4iWgjUeNx4udsw7l4jy4k130_assertion wasGeneratedBy ECO_0000203 NP473646.RAA-6NVKN5ruhURZRMZ1ggkb4iWgjUeNx4udsw7l4jy4k130_provenance.