Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_provenance.
- NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_assertion description "[Mutations in the RAF1 are associated with Noonan syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_provenance.
- NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_assertion evidence source_evidence_literature NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_provenance.
- NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_assertion SIO_000772 19020799 NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_provenance.
- NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_assertion wasDerivedFrom lhgdn-20090331 NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_provenance.
- NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_assertion wasGeneratedBy ECO_0000203 NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP123469.RA0gRSN6LhpACCdcYqp-RoYSTGxX-QP1He9QJS3aQx-zc130_provenance.