Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3389.RAxF7VVju6DxakKYegG7WFoyXiqqJoMGNS5PLouoNvVLU130_assertion> ?p ?o ?g. }
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- NP3389.RAxF7VVju6DxakKYegG7WFoyXiqqJoMGNS5PLouoNvVLU130_assertion type Assertion NP3389.RAxF7VVju6DxakKYegG7WFoyXiqqJoMGNS5PLouoNvVLU130_head.
- NP3389.RAxF7VVju6DxakKYegG7WFoyXiqqJoMGNS5PLouoNvVLU130_assertion wasGeneratedBy ECO_0000218 NP3389.RAxF7VVju6DxakKYegG7WFoyXiqqJoMGNS5PLouoNvVLU130_provenance.
- NP3389.RAxF7VVju6DxakKYegG7WFoyXiqqJoMGNS5PLouoNvVLU130_assertion wasDerivedFrom uniprot-20150221 NP3389.RAxF7VVju6DxakKYegG7WFoyXiqqJoMGNS5PLouoNvVLU130_provenance.
- NP3389.RAxF7VVju6DxakKYegG7WFoyXiqqJoMGNS5PLouoNvVLU130_assertion SIO_000772 10339581 NP3389.RAxF7VVju6DxakKYegG7WFoyXiqqJoMGNS5PLouoNvVLU130_provenance.
- NP3389.RAxF7VVju6DxakKYegG7WFoyXiqqJoMGNS5PLouoNvVLU130_assertion evidence source_evidence_curated NP3389.RAxF7VVju6DxakKYegG7WFoyXiqqJoMGNS5PLouoNvVLU130_provenance.
- NP3389.RAxF7VVju6DxakKYegG7WFoyXiqqJoMGNS5PLouoNvVLU130_assertion description "[Mutations in HYAL1, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3389.RAxF7VVju6DxakKYegG7WFoyXiqqJoMGNS5PLouoNvVLU130_provenance.