Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_provenance.
- NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_assertion description "[Craniofrontonasal syndrome (CFNS [MIM 304110]) is an X-linked malformation syndrome characterized by craniofrontonasal dysplasia and extracranial manifestations in heterozygous females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_provenance.
- NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_assertion evidence source_evidence_literature NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_provenance.
- NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_assertion SIO_000772 17941886 NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_provenance.
- NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_assertion wasDerivedFrom befree-20140225 NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_provenance.
- NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_assertion wasGeneratedBy ECO_0000203 NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP689051.RAsaSlNkLPB_K1oqPFe25L0DTiFKQm4lx5a9vPkDw07CU130_provenance.