Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_provenance.
- NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_assertion wasGeneratedBy ECO_0000203 NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_provenance.
- NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_assertion wasDerivedFrom befree-20150227 NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_provenance.
- NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_assertion SIO_000772 23786871 NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_provenance.
- NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_assertion evidence source_evidence_literature NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_provenance.
- NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_assertion description "[RASopathies (Noonan syndrome (NS) and Noonan-related syndromes) are neurodevelopmental syndromes resulting from germline mutations in genes that participate in the rat sarcoma/mitogen-activated protein kinases (RAS/MAPK) pathway (PTPN11, SOS1, RAF, KRAS or NRAS, and SHOC2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP707518.RAMuLjgV4FggOSJuFeyYMcw8dXF6RVZwNxi5vo8YavBuQ130_provenance.