Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1362964.RAxp9rxtuVGNLt_O8kp5kV5NE6q4GWfy2WIu4kfMzLGMg130_provenance.