Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_provenance.
- NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_assertion description "[There is now strong evidence for the implication of collagen alpha 1(I), alpha 2(I) and alpha 1(III) mutations in many forms of osteogenesis imperfecta and inherited arterial aneurysms (Ehlers Danlos syndrome type IV).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_provenance.
- NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_assertion evidence source_evidence_literature NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_provenance.
- NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_assertion SIO_000772 2572730 NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_provenance.
- NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_assertion wasDerivedFrom befree-20140225 NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_provenance.
- NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_assertion wasGeneratedBy ECO_0000203 NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_provenance.
- befree-20140225 importedOn "2014-02-25" NP795116.RAdjy8o-UzLVWXm2bJfKTgiKEwCo404ciciNr_JUX4ols130_provenance.