Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_provenance.
- NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_assertion description "[Identification of loss-of-function mutations of SLC35D1 in patients with Schneckenbecken dysplasia, but not with other severe spondylodysplastic dysplasias group diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_provenance.
- NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_assertion evidence source_evidence_literature NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_provenance.
- NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_assertion SIO_000772 19508970 NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_provenance.
- NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_assertion wasDerivedFrom befree-20150227 NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_provenance.
- NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_assertion wasGeneratedBy ECO_0000203 NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP869605.RAWq3Ul3Q05pMX0Xh3MxcyQ8K3HWPyGQBuUoooGYp-eLI130_provenance.