Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_assertion> ?p ?o ?g. }
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- NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_assertion type Assertion NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_head.
- NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_assertion description "[The Wiskott-Aldrich syndrome (WAS), an X-linked immunodeficiency disease caused by mutation in the recently isolated gene encoding WAS protein (WASP), is known to be associated with extensive clinical heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_provenance.
- NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_assertion evidence source_evidence_literature NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_provenance.
- NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_assertion SIO_000772 8931701 NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_provenance.
- NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_assertion wasDerivedFrom befree-2016 NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_provenance.
- NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_assertion wasGeneratedBy ECO_0000203 NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_provenance.