Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_provenance.
- NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_assertion description "[Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_provenance.
- NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_assertion evidence source_evidence_literature NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_provenance.
- NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_assertion SIO_000772 19206169 NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_provenance.
- NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_assertion wasDerivedFrom gad-20150221 NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_provenance.
- NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_assertion wasGeneratedBy ECO_0000203 NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP140691.RAGh9Oaa1vjXJ8_Pi4BEpeLkWQeIe3F5UFPJxrtE1n8qo130_provenance.