Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP719406.RALt8IswT0i4o4XmqXlwBkTIhSN7Ix7NUPImhwdYFw5CA130_provenance.