Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_provenance.
- NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_assertion wasGeneratedBy ECO_0000203 NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_provenance.
- NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_assertion wasDerivedFrom befree-20150227 NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_provenance.
- NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_assertion SIO_000772 20949621 NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_provenance.
- NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_assertion evidence source_evidence_literature NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_provenance.
- NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_assertion description "[Germline KRAS mutations were shown recently to be associated with developmental disorders, including Noonan syndrome (NS), cardio-facio-cutaneous syndrome (CFCS), and Costello syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528054.RAv_GPE3V6det1gXOzeTYXjU89dDzFdG1X9i7tTZ05I7o130_provenance.