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- source_evidence_literature type ECO_0000212 NP788769.RAM4tXUsD16x9R-PWuTkyeqGl65OfWB91qNRdx032j6Rk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788769.RAM4tXUsD16x9R-PWuTkyeqGl65OfWB91qNRdx032j6Rk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788769.RAM4tXUsD16x9R-PWuTkyeqGl65OfWB91qNRdx032j6Rk130_provenance.
- NP788769.RAM4tXUsD16x9R-PWuTkyeqGl65OfWB91qNRdx032j6Rk130_assertion description "[These results suggest that clinical manifestations in SHOC2 mutation-positive patients partially overlap with those in patients with typical Noonan or CFC syndrome and show that easily pluckable/loose anagen hair is distinctive in SHOC2 mutation-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788769.RAM4tXUsD16x9R-PWuTkyeqGl65OfWB91qNRdx032j6Rk130_provenance.
- NP788769.RAM4tXUsD16x9R-PWuTkyeqGl65OfWB91qNRdx032j6Rk130_assertion evidence source_evidence_literature NP788769.RAM4tXUsD16x9R-PWuTkyeqGl65OfWB91qNRdx032j6Rk130_provenance.
- NP788769.RAM4tXUsD16x9R-PWuTkyeqGl65OfWB91qNRdx032j6Rk130_assertion SIO_000772 20882035 NP788769.RAM4tXUsD16x9R-PWuTkyeqGl65OfWB91qNRdx032j6Rk130_provenance.
- NP788769.RAM4tXUsD16x9R-PWuTkyeqGl65OfWB91qNRdx032j6Rk130_assertion wasDerivedFrom befree-20150227 NP788769.RAM4tXUsD16x9R-PWuTkyeqGl65OfWB91qNRdx032j6Rk130_provenance.
- NP788769.RAM4tXUsD16x9R-PWuTkyeqGl65OfWB91qNRdx032j6Rk130_assertion wasGeneratedBy ECO_0000203 NP788769.RAM4tXUsD16x9R-PWuTkyeqGl65OfWB91qNRdx032j6Rk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788769.RAM4tXUsD16x9R-PWuTkyeqGl65OfWB91qNRdx032j6Rk130_provenance.