Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP329562.RAX45XrGRDDl_7_Bto8UIoAh_s2_4tIjuPXn5gUnd3QcI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP329562.RAX45XrGRDDl_7_Bto8UIoAh_s2_4tIjuPXn5gUnd3QcI130_assertion type Assertion NP329562.RAX45XrGRDDl_7_Bto8UIoAh_s2_4tIjuPXn5gUnd3QcI130_head.
- NP329562.RAX45XrGRDDl_7_Bto8UIoAh_s2_4tIjuPXn5gUnd3QcI130_assertion description "[In the current study, we report the identification of a novel disease-causing mutation in the ASAH1 gene that results in Farber disease in an Indian family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329562.RAX45XrGRDDl_7_Bto8UIoAh_s2_4tIjuPXn5gUnd3QcI130_provenance.
- NP329562.RAX45XrGRDDl_7_Bto8UIoAh_s2_4tIjuPXn5gUnd3QcI130_assertion evidence source_evidence_literature NP329562.RAX45XrGRDDl_7_Bto8UIoAh_s2_4tIjuPXn5gUnd3QcI130_provenance.
- NP329562.RAX45XrGRDDl_7_Bto8UIoAh_s2_4tIjuPXn5gUnd3QcI130_assertion SIO_000772 16951918 NP329562.RAX45XrGRDDl_7_Bto8UIoAh_s2_4tIjuPXn5gUnd3QcI130_provenance.
- NP329562.RAX45XrGRDDl_7_Bto8UIoAh_s2_4tIjuPXn5gUnd3QcI130_assertion wasDerivedFrom befree-20140225 NP329562.RAX45XrGRDDl_7_Bto8UIoAh_s2_4tIjuPXn5gUnd3QcI130_provenance.
- NP329562.RAX45XrGRDDl_7_Bto8UIoAh_s2_4tIjuPXn5gUnd3QcI130_assertion wasGeneratedBy ECO_0000203 NP329562.RAX45XrGRDDl_7_Bto8UIoAh_s2_4tIjuPXn5gUnd3QcI130_provenance.