Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_provenance.
- NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_assertion wasGeneratedBy ECO_0000203 NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_provenance.
- NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_assertion wasDerivedFrom befree-20150227 NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_provenance.
- NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_assertion SIO_000772 20030748 NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_provenance.
- NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_assertion evidence source_evidence_literature NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_provenance.
- NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_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." NP646467.RASu8ddMEiITwzMm1ZKWmsXEKm0O437l4JDIHim1vN-vg130_provenance.