Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_provenance.
- NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_assertion wasGeneratedBy ECO_0000203 NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_provenance.
- NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_assertion wasDerivedFrom befree-20150227 NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_provenance.
- NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_assertion SIO_000772 20030748 NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_provenance.
- NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_assertion evidence source_evidence_literature NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_provenance.
- NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_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." NP644216.RAqmloL8H2_v0CQaPq3ogTHf9sc-DL8L_3OKcSnnJcr8c130_provenance.