Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_provenance.
- NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_assertion description "[Cutis laxa (CL) is a heterogeneous group of genetic and acquired disorders with at least two autosomal dominant forms caused by mutations in the elastin and fibulin-5 genes, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_provenance.
- NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_assertion evidence source_evidence_literature NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_provenance.
- NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_assertion SIO_000772 15955094 NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_provenance.
- NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_assertion wasDerivedFrom befree-20150227 NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_provenance.
- NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_assertion wasGeneratedBy ECO_0000203 NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_provenance.