Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP783167.RAT8Ps0JMWiqKdhNm9ulMN9eEBn1-tZLWc3jgD05cWhVs130_assertion> ?p ?o ?g. }
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- NP783167.RAT8Ps0JMWiqKdhNm9ulMN9eEBn1-tZLWc3jgD05cWhVs130_assertion type Assertion NP783167.RAT8Ps0JMWiqKdhNm9ulMN9eEBn1-tZLWc3jgD05cWhVs130_head.
- NP783167.RAT8Ps0JMWiqKdhNm9ulMN9eEBn1-tZLWc3jgD05cWhVs130_assertion wasGeneratedBy ECO_0000203 NP783167.RAT8Ps0JMWiqKdhNm9ulMN9eEBn1-tZLWc3jgD05cWhVs130_provenance.
- NP783167.RAT8Ps0JMWiqKdhNm9ulMN9eEBn1-tZLWc3jgD05cWhVs130_assertion wasDerivedFrom befree-2016 NP783167.RAT8Ps0JMWiqKdhNm9ulMN9eEBn1-tZLWc3jgD05cWhVs130_provenance.
- NP783167.RAT8Ps0JMWiqKdhNm9ulMN9eEBn1-tZLWc3jgD05cWhVs130_assertion SIO_000772 20030748 NP783167.RAT8Ps0JMWiqKdhNm9ulMN9eEBn1-tZLWc3jgD05cWhVs130_provenance.
- NP783167.RAT8Ps0JMWiqKdhNm9ulMN9eEBn1-tZLWc3jgD05cWhVs130_assertion evidence source_evidence_literature NP783167.RAT8Ps0JMWiqKdhNm9ulMN9eEBn1-tZLWc3jgD05cWhVs130_provenance.
- NP783167.RAT8Ps0JMWiqKdhNm9ulMN9eEBn1-tZLWc3jgD05cWhVs130_assertion description "[Germline mutations in several members of RAS/RAF/MEK/ERK pathway cause clinically similar genetic disorders, including Noonan syndrome (NS), Costello syndrome (CS) and cardio-facio-cutaneous syndrome (CFC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783167.RAT8Ps0JMWiqKdhNm9ulMN9eEBn1-tZLWc3jgD05cWhVs130_provenance.