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- source_evidence_literature type ECO_0000212 NP457731.RA8C_F-vJL7WvlrymdgOQvYTv-zHZi5E2LyvJZkdStlZs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP457731.RA8C_F-vJL7WvlrymdgOQvYTv-zHZi5E2LyvJZkdStlZs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP457731.RA8C_F-vJL7WvlrymdgOQvYTv-zHZi5E2LyvJZkdStlZs130_provenance.
- NP457731.RA8C_F-vJL7WvlrymdgOQvYTv-zHZi5E2LyvJZkdStlZs130_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." NP457731.RA8C_F-vJL7WvlrymdgOQvYTv-zHZi5E2LyvJZkdStlZs130_provenance.
- NP457731.RA8C_F-vJL7WvlrymdgOQvYTv-zHZi5E2LyvJZkdStlZs130_assertion evidence source_evidence_literature NP457731.RA8C_F-vJL7WvlrymdgOQvYTv-zHZi5E2LyvJZkdStlZs130_provenance.
- NP457731.RA8C_F-vJL7WvlrymdgOQvYTv-zHZi5E2LyvJZkdStlZs130_assertion SIO_000772 14684682 NP457731.RA8C_F-vJL7WvlrymdgOQvYTv-zHZi5E2LyvJZkdStlZs130_provenance.
- NP457731.RA8C_F-vJL7WvlrymdgOQvYTv-zHZi5E2LyvJZkdStlZs130_assertion wasDerivedFrom befree-20140225 NP457731.RA8C_F-vJL7WvlrymdgOQvYTv-zHZi5E2LyvJZkdStlZs130_provenance.
- NP457731.RA8C_F-vJL7WvlrymdgOQvYTv-zHZi5E2LyvJZkdStlZs130_assertion wasGeneratedBy ECO_0000203 NP457731.RA8C_F-vJL7WvlrymdgOQvYTv-zHZi5E2LyvJZkdStlZs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP457731.RA8C_F-vJL7WvlrymdgOQvYTv-zHZi5E2LyvJZkdStlZs130_provenance.