Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP654809.RAZ5qoQFvp2GyUm1iL9tII7oenOHU0YfvTOH94Gr4VCwM130_assertion> ?p ?o ?g. }
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- NP654809.RAZ5qoQFvp2GyUm1iL9tII7oenOHU0YfvTOH94Gr4VCwM130_assertion type Assertion NP654809.RAZ5qoQFvp2GyUm1iL9tII7oenOHU0YfvTOH94Gr4VCwM130_head.
- NP654809.RAZ5qoQFvp2GyUm1iL9tII7oenOHU0YfvTOH94Gr4VCwM130_assertion description "[Thus, atypical deletions partially overlapping with the common 1.4 Mb microdeletion interval could prove useful in identifying possible genetic modifiers in the NF1 gene region whose haploinsufficiency might promote neurofibroma growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP654809.RAZ5qoQFvp2GyUm1iL9tII7oenOHU0YfvTOH94Gr4VCwM130_provenance.
- NP654809.RAZ5qoQFvp2GyUm1iL9tII7oenOHU0YfvTOH94Gr4VCwM130_assertion evidence source_evidence_literature NP654809.RAZ5qoQFvp2GyUm1iL9tII7oenOHU0YfvTOH94Gr4VCwM130_provenance.
- NP654809.RAZ5qoQFvp2GyUm1iL9tII7oenOHU0YfvTOH94Gr4VCwM130_assertion SIO_000772 18265407 NP654809.RAZ5qoQFvp2GyUm1iL9tII7oenOHU0YfvTOH94Gr4VCwM130_provenance.
- NP654809.RAZ5qoQFvp2GyUm1iL9tII7oenOHU0YfvTOH94Gr4VCwM130_assertion wasDerivedFrom befree-2016 NP654809.RAZ5qoQFvp2GyUm1iL9tII7oenOHU0YfvTOH94Gr4VCwM130_provenance.
- NP654809.RAZ5qoQFvp2GyUm1iL9tII7oenOHU0YfvTOH94Gr4VCwM130_assertion wasGeneratedBy ECO_0000203 NP654809.RAZ5qoQFvp2GyUm1iL9tII7oenOHU0YfvTOH94Gr4VCwM130_provenance.