Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP631420.RAmmcXq-WoVpKmN_R8SoBC-nIQrlaAVlN-EsH8ZESWiIw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP631420.RAmmcXq-WoVpKmN_R8SoBC-nIQrlaAVlN-EsH8ZESWiIw130_assertion type Assertion NP631420.RAmmcXq-WoVpKmN_R8SoBC-nIQrlaAVlN-EsH8ZESWiIw130_head.
- NP631420.RAmmcXq-WoVpKmN_R8SoBC-nIQrlaAVlN-EsH8ZESWiIw130_assertion wasGeneratedBy ECO_0000203 NP631420.RAmmcXq-WoVpKmN_R8SoBC-nIQrlaAVlN-EsH8ZESWiIw130_provenance.
- NP631420.RAmmcXq-WoVpKmN_R8SoBC-nIQrlaAVlN-EsH8ZESWiIw130_assertion wasDerivedFrom befree-20140225 NP631420.RAmmcXq-WoVpKmN_R8SoBC-nIQrlaAVlN-EsH8ZESWiIw130_provenance.
- NP631420.RAmmcXq-WoVpKmN_R8SoBC-nIQrlaAVlN-EsH8ZESWiIw130_assertion SIO_000772 22121117 NP631420.RAmmcXq-WoVpKmN_R8SoBC-nIQrlaAVlN-EsH8ZESWiIw130_provenance.
- NP631420.RAmmcXq-WoVpKmN_R8SoBC-nIQrlaAVlN-EsH8ZESWiIw130_assertion evidence source_evidence_literature NP631420.RAmmcXq-WoVpKmN_R8SoBC-nIQrlaAVlN-EsH8ZESWiIw130_provenance.
- NP631420.RAmmcXq-WoVpKmN_R8SoBC-nIQrlaAVlN-EsH8ZESWiIw130_assertion description "[MKS3, encoding the transmembrane receptor meckelin, is mutated in Meckel-Gruber syndrome (MKS), an autosomal-recessive ciliopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631420.RAmmcXq-WoVpKmN_R8SoBC-nIQrlaAVlN-EsH8ZESWiIw130_provenance.