Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_provenance.
- NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_assertion description "[None of the otosclerosis patients without symphalangism had NOG mutations, indicating that NOG mutations may be restrictively found within patients with various skeletal abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_provenance.
- NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_assertion evidence source_evidence_literature NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_provenance.
- NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_assertion SIO_000772 22288654 NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_provenance.
- NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_assertion wasDerivedFrom befree-20140225 NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_provenance.
- NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_assertion wasGeneratedBy ECO_0000203 NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP614977.RAlAI3-f1-JY5S02ese8elFuPqNTqrGqMXKxX8Dz6ekvY130_provenance.