Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_assertion> ?p ?o ?g. }
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- NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_assertion type Assertion NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_head.
- NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_assertion description "[This disorder is allelic with X-linked infantile spasms (ISSX; MIM 308350) where polyalanine tract expansions are the commonly observed molecular defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_provenance.
- NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_assertion evidence source_evidence_literature NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_provenance.
- NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_assertion SIO_000772 12177367 NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_provenance.
- NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_assertion wasDerivedFrom befree-20150227 NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_provenance.
- NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_assertion wasGeneratedBy ECO_0000203 NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_provenance.