Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_provenance.
- NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_assertion description "[Mutations in major structural components of elastic fibres, especially elastin, fibrillins and fibulin-5, cause severe, often life-threatening, heritable connective tissue diseases such as Marfan syndrome, supravalvular aortic stenosis and cutis laxa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_provenance.
- NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_assertion evidence source_evidence_literature NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_provenance.
- NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_assertion SIO_000772 16893474 NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_provenance.
- NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_assertion wasDerivedFrom befree-20140225 NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_provenance.
- NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_assertion wasGeneratedBy ECO_0000203 NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP201668.RACR1AtW_mVFV4-sialuAPFJDzkR3-69M9xjrzJZ6Pe7Q130_provenance.