Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_provenance.
- NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_assertion wasGeneratedBy ECO_0000203 NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_provenance.
- NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_assertion wasDerivedFrom befree-20150227 NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_provenance.
- NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_assertion SIO_000772 17054105 NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_provenance.
- NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_assertion evidence source_evidence_literature NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_provenance.
- NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_assertion description "[To further investigate the phenotypic spectrum associated with germline HRAS mutations and characterize their molecular diversity, subjects with a diagnosis of CS (N = 9), Noonan syndrome (NS; N = 36), cardiofaciocutaneous syndrome (CFCS; N = 4), or with a phenotype suggestive of these conditions but without a definitive diagnosis (N = 12) were screened for the entire coding sequence of the gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465284.RAV-nxhWItDp3n7gMcWVx7qFmh1gRUZVs-lZUmsi-zn0o130_provenance.