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- source_evidence_literature type ECO_0000212 NP269914.RAy8ZXsNbXyd12HCvfbrYqmh_u3ial0yFGMCS2wWYXX6s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269914.RAy8ZXsNbXyd12HCvfbrYqmh_u3ial0yFGMCS2wWYXX6s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269914.RAy8ZXsNbXyd12HCvfbrYqmh_u3ial0yFGMCS2wWYXX6s130_provenance.
- NP269914.RAy8ZXsNbXyd12HCvfbrYqmh_u3ial0yFGMCS2wWYXX6s130_assertion description "[Future studies should focus on detailed molecular analysis of the common cellular pathways disrupted by mutations of ALK-1 and BMPR2 that cause inherited pulmonary vascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269914.RAy8ZXsNbXyd12HCvfbrYqmh_u3ial0yFGMCS2wWYXX6s130_provenance.
- NP269914.RAy8ZXsNbXyd12HCvfbrYqmh_u3ial0yFGMCS2wWYXX6s130_assertion evidence source_evidence_literature NP269914.RAy8ZXsNbXyd12HCvfbrYqmh_u3ial0yFGMCS2wWYXX6s130_provenance.
- NP269914.RAy8ZXsNbXyd12HCvfbrYqmh_u3ial0yFGMCS2wWYXX6s130_assertion SIO_000772 14684682 NP269914.RAy8ZXsNbXyd12HCvfbrYqmh_u3ial0yFGMCS2wWYXX6s130_provenance.
- NP269914.RAy8ZXsNbXyd12HCvfbrYqmh_u3ial0yFGMCS2wWYXX6s130_assertion wasDerivedFrom befree-20150227 NP269914.RAy8ZXsNbXyd12HCvfbrYqmh_u3ial0yFGMCS2wWYXX6s130_provenance.
- NP269914.RAy8ZXsNbXyd12HCvfbrYqmh_u3ial0yFGMCS2wWYXX6s130_assertion wasGeneratedBy ECO_0000203 NP269914.RAy8ZXsNbXyd12HCvfbrYqmh_u3ial0yFGMCS2wWYXX6s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP269914.RAy8ZXsNbXyd12HCvfbrYqmh_u3ial0yFGMCS2wWYXX6s130_provenance.