Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_provenance.
- NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_assertion description "[De novo and inherited mutations in COL4A2, encoding the type IV collagen ?2 chain cause porencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_provenance.
- NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_assertion evidence source_evidence_literature NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_provenance.
- NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_assertion SIO_000772 22209246 NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_provenance.
- NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_assertion wasDerivedFrom befree-20140225 NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_provenance.
- NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_assertion wasGeneratedBy ECO_0000203 NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP749612.RAmlMHEIGmX819BTydFcZRZ_rLRSEc4-ThRIsxHjmifwk130_provenance.