Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP856887.RAx39eRttSnatpQAqwNBTuoT77PId1hdpQnwat9IhRH3w130_assertion> ?p ?o ?g. }
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- NP856887.RAx39eRttSnatpQAqwNBTuoT77PId1hdpQnwat9IhRH3w130_assertion type Assertion NP856887.RAx39eRttSnatpQAqwNBTuoT77PId1hdpQnwat9IhRH3w130_head.
- NP856887.RAx39eRttSnatpQAqwNBTuoT77PId1hdpQnwat9IhRH3w130_assertion description "[The phenotypic overlap was explained by the involvement of the Ras pathway in both disorders, and, accordingly, clustering of the NF1 mutations in the GTPase-activating protein (GAP) domain of neurofibromin was observed in individuals with NFNS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856887.RAx39eRttSnatpQAqwNBTuoT77PId1hdpQnwat9IhRH3w130_provenance.
- NP856887.RAx39eRttSnatpQAqwNBTuoT77PId1hdpQnwat9IhRH3w130_assertion evidence source_evidence_literature NP856887.RAx39eRttSnatpQAqwNBTuoT77PId1hdpQnwat9IhRH3w130_provenance.
- NP856887.RAx39eRttSnatpQAqwNBTuoT77PId1hdpQnwat9IhRH3w130_assertion SIO_000772 19449407 NP856887.RAx39eRttSnatpQAqwNBTuoT77PId1hdpQnwat9IhRH3w130_provenance.
- NP856887.RAx39eRttSnatpQAqwNBTuoT77PId1hdpQnwat9IhRH3w130_assertion wasDerivedFrom befree-20140225 NP856887.RAx39eRttSnatpQAqwNBTuoT77PId1hdpQnwat9IhRH3w130_provenance.
- NP856887.RAx39eRttSnatpQAqwNBTuoT77PId1hdpQnwat9IhRH3w130_assertion wasGeneratedBy ECO_0000203 NP856887.RAx39eRttSnatpQAqwNBTuoT77PId1hdpQnwat9IhRH3w130_provenance.