Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_provenance.
- NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_assertion description "[We performed mutation analysis of FLNA in 120 patients, of whom 72 (60%) had classical bilateral PNH and 48 (40%) other PH phenotypes, and identified 25 mutations in 40 individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_provenance.
- NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_assertion evidence source_evidence_literature NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_provenance.
- NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_assertion SIO_000772 16684786 NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_provenance.
- NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_assertion wasDerivedFrom befree-20140225 NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_provenance.
- NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_assertion wasGeneratedBy ECO_0000203 NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP560212.RA7HyOMkPqmTl_qKGPslQHteB4GYprPY1tbuZWCqD2NRo130_provenance.